GENETIC TESTS
Our Goal for Genetic Tests is enable it as a blueprint for Precision Health Guidance
Precision health test aims to offer personalized healthcare solutions by considering an individual’s distinct genetic makeup, environmental factors, lifestyle choices, and other personal characteristics.
Our essential goals for precision health is to Determine personalized care for every individual customer, Detect disease mutations that may be responsible for undiagnosed conditions. Prevent serious medication side effects. Identify genetic risk factors to provide lifestyle/environmental recommendations that can enhance the health of each patient.
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Men's Health Panel
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Women's Health Panel
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Pediatric panel
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Breast Cancer Panel
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Allergies Panel
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Fertility Panel
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Dental Panel
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Neurodegenerative Panel
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Antioxidants, Vitamins and Minerals
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Gastrointestinal Disease Panel
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Oncologic Panel
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Sports Panel
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Panel of Gynecology and Obstetrics
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Ophthalmology panel
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Skin panel
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Orthopedics and Rheumatology Panel
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Autoimmune Disease Panel
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Hematology panel
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Genetic disorders Panel
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Endocrinology and Metabolism Panel
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Susceptibility to Coronavirus
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Life Hormones Panel
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Microbiome Panel
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Nutrition Panel
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Facial Harmonization
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Inflammations
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TEA (version 3.0) - Updated 12.06.2021
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Diabetes
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MTHFR
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Behavioral
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Hair
Categories
Conditions Observed
Cardio-Circulatory System | Atherosclerosis |
Hypertension (High Blood Pressure) | |
Acute myocardial infarction | |
Cholesterol Level (HDL) | |
Panel | |
Triglycerides | |
Venous Thrombosis | |
Cardiac Arrhythmia | |
High Ferritin | |
Heart disease | |
Ischemic Stroke | |
MTHFR 1298 mutation (rs1801131) | |
MTHFR 677 mutation (rs1801133) | |
Neurological System | Mental and Cognitive Decline (Age) |
Stroke | |
Alzheimer’s disease | |
Parkinson’s disease | |
Sleep Quality | |
Dopamine Synthesis | |
Serotonin Synthesis | |
Fertility | Male infertility |
Behavioral | Anxiety |
Seletividade em Relacionamento | |
Impulsivity | |
Fears | |
Mood Disorder | |
Depression | |
Difficulties in Receiving Reviews | |
Gastrointestinal System | Gluten Intolerance |
Lactose intolerance | |
Ulcerative Colitis | |
Leaky Gut Syndrome | |
Milk Protein Allergy | |
Irritable Bowel Syndrome | |
Ulcer | |
Celiac disease | |
Gastritis | |
Oncology | Thyroid Neoplasm |
Colorectal Neoplasm | |
Prostate Neoplasm | |
Skin Cancer | |
Lungs Cancer | |
Respiratory system | Asthma |
Flu (Influenza) | |
Bronchitis | |
Apnea | |
Pulmonary emphysema | |
Allergic Rhinitis | |
Genito-Urinary System | Kidney Calculus |
Benign Prostate Hyperplasia | |
Osteo-Muscular System | Osteoporosis |
Rheumatoid arthritis | |
Arthrosis of the Knee | |
Disc herniation | |
Endocrinological System – Disease Susceptibility | Metabolic syndrome |
Autoimmune Thyroid Disease | |
Insulin Resistance | |
Type 2 diabetes | |
Hypothyroidism | |
Endocrinological System – Hormones | Oxytocin |
Melatonin | |
Insulin | |
Cortisol | |
DHEA/DHEAS | |
Progesterone | |
Testosterone | |
Dihydrotestosterone | |
Sensory System | Cataract |
Age Related Macular Degeneration | |
Glaucoma | |
Myopia | |
Hyperopia | |
Astigmatism | |
Deafness | |
Allergies | Food Coloring Allergy |
Allergies in General |
Categories
Conditions observed
Immune system | MTHFR 677 mutation (rs1801133) |
MTHFR 1298 mutation (rs1801131) | |
Accumulation of Homocysteine | |
Glycation | |
Allergies in General | |
Allergy to Food Coloring | |
Cardio-Circulatory System | High Ferritin |
Atherosclerosis | |
Heart disease | |
Hypertension (High Blood Pressure) | |
Acute myocardial infarction | |
Venous Thrombosis | |
Ischemic Stroke | |
Cardiac Arrhythmia | |
Cholesterol Level (HDL) | |
Cholesterol Level (LDL) | |
Triglycerides | |
Behavioral | Depression |
Relationship Difficulty | |
Difficulties in Receiving Reviews | |
Impulsivity | |
Fears | |
Selectivity on Relationships | |
Mood Disorder | |
Anxiety | |
Oncology | Thyroid Neoplasm |
Colorectal Neoplasm | |
Breast neoplasm | |
Ovary Neoplasm | |
Endometrial Neoplasm | |
Lungs Cancer | |
Skin Cancer | |
Osteo-Muscular System | Osteoporosis |
Rheumatoid arthritis | |
Arthrosis of the Knee | |
Disc herniation | |
Genito-Urinary System | Kidney Calculus |
Candidiasis | |
Polycystic Ovary Syndrome | |
Endometriosis | |
Uterine Fibroids | |
Recurrent Urinary Tract Infection | |
Gastrointestinal System | Crohn’s disease |
Lactose intolerance | |
Ulcerative Colitis | |
Leaky Gut Syndrome | |
Constipation | |
Celiac disease | |
Gluten Intolerance | |
Irritable bowel syndrome | |
Milk Protein Allergy | |
Biliary Calculations | |
Ulcer | |
Gastritis | |
Fertility | Lower Sexual Desire (Female) |
In vitro fertilization | |
Female Infertility | |
Pregnancy | |
Pregnancy sickness | |
Thyrotoxicosis | |
Recurring Gestational Loss (lower risk) | |
Intra-Hepatic Pregnancy Cholestasis | |
Uterine Fibromyoma | |
Neural Tube Defect | |
Miscarriages | |
Protein C Deficiency | |
Antithrombin Deficiency | |
Antiphospholipid Antibody Syndrome | |
Mutation of the SERPINE1 Gene (PAI-1) | |
Protein S deficiency | |
Isolated Follicle Stimulating Hormone (FSH) Deficiency | |
Fragile X Syndrome | |
FSH deficiency | |
Neurological System | Mental and Cognitive Decline (Age) |
Stroke | |
Parkinson’s disease | |
Sleep Quality | |
Dopamine Synthesis | |
Serotonin Synthesis | |
Alzheimer’s disease | |
Endocrinological System – Disease Susceptibility | Hypothyroidism |
Type 2 diabetes | |
Metabolic syndrome | |
Insulin Resistance | |
Hashimoto’s Thyroiditis | |
Endocrinological System – Hormones | Oxytocin |
Melatonin | |
Insulin | |
Cortisol | |
DHEA/DHEAS | |
Testosterone | |
Progesterone | |
Estradiol | |
Respiratory system | Pulmonary emphysema |
Apnea | |
Asthma | |
Bronchitis | |
Flu (Influenza) | |
Allergic Rhinitis | |
Sensory System | Cataract |
Age Related Macular Degeneration | |
Glaucoma | |
Deafness | |
Myopia | |
Hyperopia | |
Astigmatism |
Categories
Conditions Observed
Allergies | Allergic Rhinitis |
Allergies in General | |
Allergy to Pets | |
Allergy to mites | |
Allergy to pollen | |
Asthma | |
Atopic Dermatitis | |
Cockroach allergy | |
Contact dermatitis | |
Eczema | |
Egg White Allergy | |
Grass allergy | |
Histamine Intolerance | |
Milk Allergy | |
Peanut Allergy | |
Sensitivity to secondhand smoke | |
Auditory system | Non-syndromic deafness |
Otitis | |
Behavioral Changes | Aggressiveness |
Neuroticism | |
Benefits | Optimism Trend |
Cancer | Childhood Leukemia |
Retinoblastoma | |
Cardiovascular | Aortic stenosis |
Cardiac Arrhythmia | |
Cardiovascular Disease (Cholesterol Level) | |
Familial Hyperlipoproteinemia Type III | |
Hereditary familial hypercholesterolemia | |
Hypercholesterolemia (Type B) | |
Dentistry | Caries |
Periodontitis | |
Teeth development | |
Diabetes | Early Type 2 Diabetes |
Type 1 Diabetes | |
Type 2 diabetes | |
Digestive system | Canker sores |
Cystic fibrosis | |
Drug Reactions | Vaccine Reactions |
Endocrine system | Hashimoto’s Thyroiditis |
Hashimoto’s Thyroiditis (in children) | |
Hypothyroidism | |
General | Aversion to Vegetables and Coffee |
Bacterial Meningitis | |
Williams Syndrome | |
Genetic diseases | Angelman Syndrome |
Blepharophimosis Syndrome | |
Char syndrome | |
Cockayne’s Syndrome | |
Hyperornithinemia-Hyperammonemia-Homocitrulinuria Syndrome | |
Kabuki Syndrome | |
Marfan syndrome | |
Miller-Dieker Syndrome | |
Mucopolysaccharidosis Type VI | |
PANDAS Syndrome | |
Phelan-McDermid Syndrome | |
Prader-Willi Syndrome | |
Rett Syndrome | |
Smith-Magenis Syndrome | |
Treacher-Collins Syndrome | |
Type 0B Glycogenosis | |
Ubiquitins | |
Hematologic system | Anemia |
HDL (Cholesterol) | |
Hemolytic Anemia | |
Low ferritin in children under 2 years | |
Spherocytosis | |
Triglycerides | |
Hormone | Folic Acid Metabolism |
Growth Hormone (GH) Deficiency | |
Hormones | Aromatase Deficiency |
Immune system | Allergy to Food Colors |
Chronic adenoiditis | |
HLA-DQ2.2 | |
HLA-DQ2.5 | |
HLA-DQ4 | |
HLA-DQ7 | |
HLA-DQ8 | |
Tonsillitis | |
Internalizations | Anxiety |
Depression | |
Internalizing Disorder | |
Metabolic | Celiac disease |
Lactose intolerance | |
Methylenetetrahydrofolate reductase (MTHFR) deficiency | |
Obesity | |
Trend of Eating Sweets | |
Metabolic disorders | Cerebrotendinous Xanthomatosis (CTX) |
Muscular system | Becker Muscular Dystrophy |
Dystonia | |
Need for Nutrients | Iodine |
Neurological | Motor coordination |
Rolandic Epilepsy | |
West syndrome | |
Pains | Headache |
Pediatric | Delayed Motor Development |
Neonatal Mortality | |
Personal characteristics | Attention deficit |
Circadian Rhythm Impact | |
Cognitive Flexibility | |
Cognitive empathy | |
Creativity | |
Greater Stimulus with Caffeine | |
Height | |
Hyperactivity | |
Increased Environmental Sensitivity | |
Manual dexterity | |
Memory | |
Memory (long term, logic) | |
Memory (traumatic) | |
Memory (verbal) | |
Obsessive-Compulsive Disorder (OCD) | |
Physical resistance | |
Sense of Taste (Bitter) | |
Skill in Mathematics | |
Sociability | |
Susceptibility to Bacteria | |
Tendency to sleep late | |
Visuospatial Working Memory | |
Worst Social Interaction in Autism | |
Worst Verbal Communication in Autism | |
Provocative | Oppositional defiant disorder (ODD) |
Psychiatric | Addiction tendency (eating, gambling, alcohol, smoking) |
Anorexia Nervosa | |
Attention Deficit Hyperactivity Disorder (ADHD) | |
Autism (Asperger’s Syndrome) | |
Autism Spectrum Disorder (ASD) | |
Autism Visual Endophenotype | |
Cataplexy and Narcolepsy (sleep) | |
Cognitive skills, attention and memory | |
Dyslexia | |
Face Recognition Memory | |
Intelligence (higher IQ if breastfed) | |
Intelligence – IQ | |
Language disorder | |
Motion sickness | |
Non-syndromic Intellectual Disability | |
Openness to New Experiences | |
RBFOX1 gene | |
Restless Legs Syndrome (Willis-Ekbom disease) | |
Shyness | |
Type A Personality | |
Type D Personality | |
Reproductive system | Male precocious puberty |
Respiratory system | Interstitial Lung Disease |
Respiratory Syncytial Virus (RSV) | |
Skeletal system (bones) | Atelosteogenesis |
Hypochondroplasia | |
Musculoskeletal Pain | |
Scoliosis | |
Skin | Acne |
Urinary system | Chronic Kidney Disease |
Nephroliathiasis in children | |
Nephrotic syndrome | |
Renal agenesis | |
Smaller Kidneys in Newborns | |
Vision (Ophthalmology) | Astigmatism |
Myopia | |
Vitamins | Vitamin D |
Vitamins need | Biotinidase Deficiency |
Weight | Binge Eating Disorder |
Obesity in Adolescents |
Categories
Conditions Observed
Benefit | Benefits of Coffee in Reducing the Risk of Breast Cancer |
Breast cancer | Breast Cancer Prognosis (HR+) |
Breast Neoplasm (Family) | |
Breast neoplasm | |
Ductal Carcinoma (Breast) | |
ER-positive (HR+) Breast Cancer | |
Estrogen sensitive breast cancer | |
HER2 Positive (HER2+) BC | |
PR-positive (HR+) breast cancer | |
Post-Menopause Breast Neoplasm | |
Cancer | Cervical Cancer |
Cowden’s Syndrome | |
Disease Free Survival (DFS) | |
Endometrial Neoplasm | |
Higher Mammographic Density | |
Metastasis | |
Neoplasms (General Risk) | |
Ovary Neoplasm | |
Triple Negative (RH-, HER2-) | |
Triple positive (RH+, HER2+) | |
Genes | BRCA1 |
BRCA2 | |
Genetic diseases | Hereditary Breast and Ovary Cancer Syndrome |
Hormone | Adiponectin Flag |
Hormones | Aromatase Deficiency |
Progesterone | |
Oxidation | Oxidative stress |
Personal characteristics | Tendency to Larger Breasts |
Tendency to have smaller breasts | |
Reactions to Treatments | Breast Cancer risk associated with estrogen-progesterone combination therapy (EPT) |
Reproductive system | Endometriosis |
Polycystic Ovary Syndrome | |
Uterine Fibroids | |
Uterine Fibromyoma |
Categories
Conditions Observed
Allergies | Allergic Asthma |
Allergic Rhinitis | |
Allergies in General | |
Allergy to Hydrolyzed Wheat Protein | |
Allergy to Nuts | |
Allergy to Pets | |
Allergy to Shrimp | |
Allergy to mites | |
Allergy to pollen | |
Aspirin Exacerbated Respiratory Disease (AERD) | |
Asthma | |
Atopic Dermatitis | |
Cockroach allergy | |
Cold-induced hives | |
Contact dermatitis | |
Dermographism | |
Eczema | |
Egg White Allergy | |
Grass allergy | |
Histamine Intolerance | |
IgE | |
Mast Cell Activation Syndrome (MCAS) | |
Milk Allergy | |
Peach Allergy | |
Peanut Allergy | |
Reaction to Paraben | |
Reaction to Phthalates | |
Reaction to Triclosan | |
Sensitivity to secondhand smoke | |
Cardiovascular | Sensitivity to Vehicle Pollution |
Genetic diseases | Congenital Ichthyosis |
Immune system | Allergy to Food Colors |
Food Allergy | |
Psoriasis | |
Metabolic | Celiac disease |
Gluten Intolerance | |
Lactose intolerance | |
Sensitivity to Caffeine | |
Metabolic disorders | Fructosemia |
Need for Nutrients | Quercetin |
Psychiatric | Misophony |
Motion sickness | |
Reactions to Treatments | Glucocorticoid Resistance |
Glucocorticoid Therapy | |
Respiratory system | Aspergillosis |
Rhinosinusitis | |
Skin | Alcohol Erythema Reaction |
Erythema | |
Histamine | |
Ichthyosis | |
Inflammatory Skin Response | |
Rosacea |
Categories
Conditions Observed
Breast cancer | Ductal Carcinoma (Breast) |
Cancer | Ovary Neoplasm |
Testicular Neoplasm | |
Cardiovascular | Prothrombin (G20210A Mutation) |
Digestive system | Constipation |
Familial Intrahepatic Cholestasis | |
Drug Reactions | Congenital Heart Defect due to Maternal Periconception – SSRIs |
Reactions with the use of antidepressants (SSRI) | |
Endocrine system | Hyperthyroidism |
Thyrotoxicosis | |
Transient Neonatal Diabetes | |
General | Longer Menstrual Cycle Duration |
Menstrual Migraine | |
Hematologic system | Congenital afibrinogenemia |
Hereditary diseases | Fragile X Syndrome |
Hormone | Anti-Müllerian hormone (AMH) |
Dihydrotestosterone (DHT) | |
FSH deficiency | |
Luteinizing Hormone (LH) | |
SHBG levels | |
Hormones | Estradiol |
Inhibin | |
Isolated Follicle Stimulating Hormone Deficiency (FSH) | |
Testosterone | |
Immune system | Anti-Beta-2-Glycoprotein Antibody |
Antiphospholipid Antibody Syndrome | |
Antithrombin Deficiency | |
Defect in Thyroid Hormonogenesis | |
Factor V Leiden Mutation | |
Mutation of the SERPINE1 Gene (PAI-1) | |
Prolactin Promoter Polymorphism | |
Protein C Deficiency | |
Protein S Deficiency | |
Metabolic | Ceruloplasmin |
Methylation | MTHFR 1298 mutation (rs1801131) |
MTHFR 677 mutation (rs1801133) | |
Psychiatric | Postpartum depression |
Reproductive system | Azoospermia |
Azoospermia não obstrutiva | |
Endometriosis | |
Erectile Dysfunction | |
Erectile Dysfunction after Radiotherapy for Prostate Cancer | |
FSH levels | |
Female Infertility | |
Gestational diabetes | |
In vitro fertilization | |
Increased Excitation Levels | |
Infertility in Endometriosis | |
Intra-Hepatic Pregnancy Cholestasis | |
Male infertility | |
Male precocious puberty | |
Neural Tube Defect | |
Oligozoospermia | |
Ovarian Hyperstimulation Syndrome | |
Ovarian Response to Hormonal Stimulation | |
Pelvic Organ Prolapse | |
Peyronie’s disease | |
Polycystic Ovary Syndrome | |
Pregnancy | |
Premature Ovarian Insufficiency | |
Risk of Recurring Pregnancy Loss | |
Sexual Motivation (Female) | |
Spermatocele | |
Spontaneous abortions | |
Teratozoospermia | |
Uterine Fibroids | |
Uterine Fibromyoma | |
Skeletal system (bones) | Development Defects |
Skin | Hereditary Chronic Mucocutaneous Candidiasis |
Vitamins need | Riboflavin Deficiency |
Categories
Conditions Observed
Cancer | Oral Cavity and Laryngeal Neoplasm |
Dentistry | Aggressive Periodontitis |
Amelogenesis imperfecta (teeth) | |
Bone demineralization in the dental arch | |
Bone resorption for prosthesis implants | |
Bruxism | |
Caries | |
Dental Fluorosis | |
Dental erosion | |
Dental implant failure | |
Dentinogenesis Imperfecta | |
Duration of orthodontic treatment after premolar extraction | |
Effectiveness in response to bisphosphonates | |
Enamel hypoplasia | |
Endodontic treatment failure | |
External apical root resorption after orthodontic treatment | |
Gingivitis | |
Incisor Molar Hypomerization (HMI) | |
Increased bleeding in chronic periodontitis | |
Inflammatory and infectious endocarditis | |
Orofacial pain | |
Periodontitis | |
Persistent Apical Periodontitis | |
Pulpitis (Tooth Inflammation) | |
Resistance to demineralization of dental enamel | |
Shovel-shaped incisor teeth | |
Teeth development | |
Temporomandibular disorder | |
Third molar agenesis | |
Tooth Agenesis | |
Digestive system | Canker sores |
Genetic diseases | Van der Woude Syndrome |
Microbiome | Dialister Species |
Categories
Conditions Observed
Amino acids | L-arginine |
Serine Deficiency | |
Antioxidants / Supplements | Coenzyme Q10 |
Retinoic Acid | |
Auditory system | Otosclerosis |
Behavioral Changes | Aggressiveness |
Cancer | Glioma |
Neuroblastoma | |
Cardiovascular | Atherosclerosis (early in children) |
Atherosclerosis (hyperlipidemia) | |
Brain aneurysm | |
Cardiovascular and Cerebrovascular | Nitric Oxide |
Stroke | |
Digestive system | Peroxisomal Enzyme Deficiency |
Fatty acids | Omega 3 |
Genetic diseases | Familial Amyloidotic Polyneuropathy (FAP) |
Familial Dysautonomy (Riley-Day Syndrome) | |
Metachromatic leukodystrophy | |
Mucopolysaccharidosis Type IIIB | |
Pseudo Arisulfatase A Deficiency | |
Salla’s disease | |
Wilson’s Disease | |
Zellweger Syndrome | |
Hematologic system | Argininemia |
Creatinophosphokinase | |
Neuroferritinopathy | |
Hereditary diseases | Friedreich’s Ataxia |
Immune system | Guillain-Barré Syndrome |
Neurofibromatosis | |
Neurosarcoidosis | |
Inflammations | C-reactive protein |
Metabolic | Mitochondrial Complex Deficiency 1 |
Metabolic disorders | Thiamine 4 Metabolism Dysfunction Syndrome |
Muscular system | Hemiplegia |
Leigh’s Syndrome | |
Need for Nutrients | Apigenin need |
Choline | |
Reaction to Glutamate | |
Turmeric (Curcumin) | |
Uridine Monophosphate | |
Neurodegenerative diseases | Alzheimer’s disease |
Alzheimer’s disease (early) | |
Amyotrophic Lateral Sclerosis (ALS) | |
Canavan disease | |
Cerebral Amyloid Angiopathy | |
Charcot-Marie Disease | |
Creutzfeldt-Jakob Disease | |
Delay of Alzheimer’s Disease in 10 years | |
Diffuse Mesangial Sclerosis | |
Ethylmalonic Encephalopathy | |
Frontotemporal Lobar Degeneration | |
Glutaric Acidemia | |
Hereditary Sensory Neuropathy | |
Huntington’s Disease | |
Louis-Bar Syndrome (Ataxia Telangiectasia) | |
Mental and Cognitive Decline (Age) | |
Molybdenum Cofactor Deficiency | |
Motor Neuropathy | |
Mucopolysaccharidosis Type IIIA | |
Multiple sclerosis | |
Neuronal Ceroid Lipofuscinosis Type 2 | |
Parkinson’s disease | |
Peripheral neuropathy | |
Pick’s Disease | |
Primary Progressive Aphasia | |
Progressive Supranuclear Palsy | |
Spinocerebellar Ataxia | |
Systemic Sclerosis | |
Tay-Sachs disease | |
Torsional dystonia | |
Vascular dementia (in elderly) | |
Wolfram Syndrome-1 | |
Neurological | BDNF |
Dopamine Receptors | |
Dopamine Synthesis | |
Dopamine conversion | |
Dopamine degradation | |
Dopamine transporters | |
GLUT1 Deficiency Syndrome | |
Increased Risk of Alzheimer’s in Diabetics (T2) | |
Mental decline with age | |
Serotonin Receptors | |
Serotonin Synthesis | |
Serotonin Transporters | |
Serotonin degradation | |
Personal characteristics | Cognitive Flexibility |
Hypothalamus Size (Smaller GG) | |
Pineal Hyperplasia | |
Visuospatial Working Memory | |
Psychiatric | Early Wake Up Time |
Schizophrenia | |
Sleep | Time to sleep later |
Vitamins | Folate |
Vitamin B3 (Niacin) |
Categories
Conditions Observed
Amino acids | N-acetylcysteine |
Antioxidants / Supplements | Coenzyme Q10 |
Glutathione | |
Probiotics | |
Retinol | |
Benefit | Benefit of Green Tea |
Chamomile | |
Passionflower (Vitexin) | |
S-adenosylmethionine (SAMe) | |
Cardiovascular and Cerebrovascular | Nitric Oxide |
Essential Amino Acids | L-methionine |
Fatty acids | Omega 3 |
Omega 6 | |
Omega 9 | |
Hormones | Benefit of Melatonin |
DHEA/DHEAS | |
Metabolic | Serum Ascorbate Levels |
Metabolic disorders | Hyperferritinemia |
Minerals | Blood Phosphate Levels |
Need for Nutrients | Apigenin |
Apigenin need | |
Bromelain | |
Calcium | |
Chrome | |
Copper | |
Hop | |
Iodine | |
Iron | |
Lutein | |
Lycopene | |
Magnesium | |
Manganese | |
Molybdenum | |
Phosphatidylcholine Levels | |
Phosphorus | |
Potassium | |
Quercetin | |
Resveratrol | |
Selenium | |
Uridine Monophosphate | |
Vitexin need | |
Zeaxanthin | |
Zinc | |
Vitamins | Beta carotene |
Folate | |
Inositol (Vitamin B8) | |
Nicotinamide (B3) | |
Reduction in Ascorbate Transport | |
Transcobalamin II Deficiency | |
Vitamin A | |
Vitamin B1 (Thiamine) | |
Vitamin B12 | |
Vitamin B12 (Levels) | |
Vitamin B2 | |
Vitamin B3 (Niacin) | |
Vitamin B5 (Pantothenic Acid) | |
Vitamin B6 | |
Vitamin B7 (Biotin) | |
Vitamin B9 (Folic Acid) | |
Vitamin C | |
Vitamin D | |
Vitamin E | |
Vitamin K | |
Vitamin K2 | |
Vitamins need | Riboflavin Deficiency |
Categories
Conditions Observed
Cancer | Biliary Pathway Neoplasm |
Colorectal Neoplasm | |
Colorectal Neoplasm (Family) | |
Colorectal Neoplasm (Meat Consumption) | |
Gallbladder Neoplasm | |
Gastrointestinal Carcinoid Tumor | |
Gastrointestinal Stromal Tumor | |
Hereditary Tyrosinemia Type 1 | |
Liver Neoplasm | |
Lynch Syndrome | |
Neoplasms (General Risk) | |
Oral Cavity and Laryngeal Neoplasm | |
Pancreas Neoplasm | |
Stomach Neoplasm | |
Cardiovascular | Arginine-succinic aciduria |
Digestive system | ABCB1 Gene Polymorphisms (MDR1) |
Alagille Syndrome (Arteriohepatic Dysplasia) | |
Amyloidosis | |
Bowel polyps | |
Canker sores | |
Chronic Hepatitis (B) | |
Chronic gastritis | |
Clostridium Difficile Infection (Patients with Ulcerative Colitis) | |
Congenital Lactase Deficiency | |
Congenital diarrhea | |
Constipation | |
Cystic fibrosis | |
Dubin-Johnson Syndrome | |
Eosinophilic Esophagitis | |
Gallstones (Vesicle) | |
Gastroesophageal Reflux Disease | |
Gastroesophageal Reflux Disease | |
Gilbert’s Syndrome | |
Hepatic Fibrosis | |
Hirschsprung’s Disease (HD) | |
Increased Susceptibility to H. pylori Infection | |
Irritable Bowel Syndrome | |
Juvenile Polyposis Syndrome | |
Non-Alcoholic Liver Steatosis | |
Pancreatitis | |
Permeable Intestine Syndrome | |
Peroxisomal Enzyme Deficiency | |
Primary Biliary Cirrhosis (CBP) | |
Trichohepatoenteric Syndrome (THE) | |
Type 1 Progressive Intrahepatic Cholestasis | |
Type 2 Progressive Intrahepatic Cholestasis | |
Type 3 Progressive Intrahepatic Cholestasis | |
Type 4 Progressive Intrahepatic Cholestasis | |
Ulcer | |
Ulcerative Colitis | |
Drug Reactions | Hepatitis caused by anti-tuberculosis drugs |
General | ALT / AST Index |
Hepatocellular Carcinoma (HCC) | |
Protein Digestive Capacity | |
Genetic diseases | Alpha-1 Antitrypsin Deficiency |
Hereditary angioedema | |
Mucolipidosis Type 4 (Gangliosidosis) | |
Peutz-Jeghers syndrome | |
Primary Hyperoxaluria | |
Wilson’s Disease | |
Zellweger Syndrome | |
Hematologic system | Albumin |
Aspartate Aminotransferase (AST) | |
Haptoglobin | |
Hemochromatosis | |
High Ferritin | |
Hyperbilirubinemia | |
Low Ferritin in Men | |
Low Ferritin in Women | |
Transferrin | |
Immune system | Crohn’s disease |
HLA-DQ2.2 | |
HLA-DQ2.5 | |
HLA-DQ4 | |
HLA-DQ7 | |
HLA-DQ8 | |
Primary Sclerosing Cholangitis | |
Inflammations | Inflammatory Bowel Disease (IBD) |
Sarcoidosis | |
Yao’s Syndrome | |
Metabolic | Celiac disease |
Ceruloplasmin | |
Gluten Intolerance | |
Lactose intolerance | |
Lipid Metabolism | |
Sensitivity to Caffeine | |
Metabolic disorders | Glycogen Storage Disease |
Hyperferritinemia | |
Low Ferritin | |
Methylmalonic Acidemia | |
Niacin’s Benefit in Reducing Liver Fat | |
Niemann-Pick Disease | |
Need for Nutrients | Molybdenum |
Reactions to Treatments | Benefit of Aspirin on colorectal cancer risk |
Glucocorticoid Resistance | |
Glucocorticoid Therapy | |
Urinary system | Focal Segmental Glomerulosclerosis |
Risk of formation of Gallstones | |
Vitamins | Vitamin B12 (Levels) |
Weight | Binge Eating Disorder |
Reduction of body fat with intervention of polyphenols |
Categories
Conditions Observed
Breast cancer | Breast Neoplasm (Family) |
Breast neoplasm | |
Ductal Carcinoma (Breast) | |
Cancer | Acute Lymphoblastic Leukemia (ALL) |
Adrenocortical Carcinoma | |
Astrocytoma | |
BAP1 – Tumor Predisposition Syndrome | |
Biliary Pathway Neoplasm | |
Bladder Neoplasm | |
Brain Neoplasm | |
Cervical Cancer | |
Cervical Neoplasm | |
Chordomas | |
Colon Carcinoma | |
Colorectal Neoplasm | |
Colorectal Neoplasm (Family) | |
Colorectal Neoplasm (Meat Consumption) | |
Craniopharyngioma | |
Diffuse large B-cell lymphoma | |
Endometrial Neoplasm | |
Follicular Lymphoma | |
Gallbladder Neoplasm | |
Gastrointestinal Carcinoid Tumor | |
Gastrointestinal Stromal Tumor | |
Glioma | |
Head and neck squamous cell carcinoma (HNSCC): | |
Hereditary Cancer Predisposition Syndrome | |
Hereditary Nonpolyposis Colorectal Neoplasm | |
Hereditary Tyrosinemia Type 1 | |
Hodgkin’s lymphoma | |
Invasive Squamous Cell Carcinoma | |
JAK2 V617F mutation | |
Li-Fraumeni Syndrome | |
Liver Neoplasm | |
Lung Neoplasm | |
Lung adenocarcinoma | |
Lynch Syndrome | |
Malignant Pleural Mesothelioma | |
Medulloblastoma | |
Meningioma | |
Metastasis | |
Multiple Endocrine Neoplasm | |
Multiple myeloma | |
Myelodysplastic Syndrome | |
Myeloproliferative Disorder | |
Nasopharyngeal Neoplasm | |
Neoplasm: Leukemia (Blood) | |
Neoplasms (General Risk) | |
Neuroblastoma | |
Non-Hodgkin’s Lymphoma | |
Non-Small Cell Lung Neoplasm | |
Oligodendroglioma | |
Oral Cavity and Laryngeal Neoplasm | |
Osteosarcoma | |
Ovary Neoplasm | |
Pancreas Neoplasm | |
Peripheral T cell lymphoma | |
Pituitary Adenoma | |
Polycythemia Vera | |
Prostate Neoplasm | |
Retinoblastoma | |
Schwannoma | |
Skin Neoplasm (Basic Cell Carcinoma – BCC) | |
Skin Neoplasm (Melanoma – Hereditary) | |
Skin Neoplasm (Melanoma) | |
Skin Neoplasm (in redheads) | |
Skin Neoplasm (light sensitivity) | |
Small Cell Lung Cancer | |
Squamous cell carcinoma | |
Stomach Neoplasm | |
Testicular Neoplasm | |
Thyroid Neoplasm | |
Tumor Carcinosis | |
Tumor Necrosis Factor Alpha | |
Tumor calcinosis | |
Tumor predisposition syndrome (BAP1) | |
Wilms’ Tumor | |
Digestive system | Bowel polyps |
Juvenile Polyposis Syndrome | |
Drug Reactions | Risk of Peripheral Neuropathy using Taxane |
General | Hepatocellular Carcinoma (HCC) |
Genes | GSTT1 |
Genetic diseases | Bloom Syndrome |
Hereditary Breast and Ovary Cancer Syndrome | |
Peutz-Jeghers syndrome | |
Proteus Syndrome | |
Rasopathies | |
Hematologic system | Idiopathic Hypereosinophilic Syndrome |
Hormone | Adiponectin Flag |
Immune system | Neurofibromatosis |
Neurodegenerative diseases | Louis-Bar Syndrome (Ataxia Telangiectasia) |
Oncologic | BRAF V600E mutation |
Choroidal Melanoma | |
Reactions to Treatments | Allogeneic Rejection |
Benefit of Aspirin on colorectal cancer risk | |
Camel Milk Benefit in Smokers | |
Chemotherapy Effectiveness | |
Fluoroucacil Response | |
Glucocorticoid Resistance | |
Glucocorticoid Therapy |
Categories
Conditions Observed
Amino acids | Beta-alanine |
L-carnitine Deficiency | |
L-glutamine | |
Monohydrate Creatine | |
Antioxidants / Supplements | BCAA levels |
Beta-Casein A1 | |
Beta-Casein A2A2 | |
Leucine Absorption | |
Retinoic Acid | |
Vegetarian Protein Shake | |
Whey Protein | |
Behaviors | Motivation to Exercise |
Persistence | |
Sports Behavior | |
Benefits | Adaptability |
Cardiovascular | Aerobic Capacity |
Brugada Syndrome | |
Cardiac Capacity | |
Familial Hypertrophic Cardiomyopathy | |
Increased blood pressure during exercise | |
Jervell and Lange-Nielsen Syndrome | |
Paroxysmal Ventricular Fibrillation | |
Romano-Ward Syndrome | |
Ventricular Tachycardia | |
Wolff-Parkinson-White Syndrome | |
Fatty acids | Arachidonic Acid Deficiency |
General | Canoeing |
Protein Digestive Capacity | |
Genetic diseases | Sudden Death Syndrome |
Walker-Warburg Syndrome | |
Hematologic system | Benefit of Physical Exercise for HDL |
High Ferritin | |
Hereditary diseases | Pompe disease |
Hormones | Cortisol Level |
DHEA/DHEAS | |
Increased Cortisol (in women) | |
Increased Noradrenaline Level During Exercise | |
Progesterone | |
Suppression of the secretion of luteinizing hormone due to anabolics | |
Testosterone | |
Injuries | Achilles tendon injury |
Anterior Cruciate Ligament Injury (ACL) | |
Best Recovery after Injury | |
Exercise Induced Muscle Damage | |
Fractures | |
Hamstring Injuries | |
Hip dislocation | |
Increased Risk of Sports Injuries | |
Ligament Rupture | |
Meniscus Injury | |
Probability of Muscle Injuries | |
Shoulder Shift | |
Sports-Related Musculoskeletal Injuries | |
Metabolic | Greater Insulin Sensitivity with Physical Exercise |
Improving Insulin Sensitivity with Physical Exercise | |
Mitochondrial Complex Deficiency 1 | |
Protein Metabolization | |
Resting Metabolic Rate | |
Resting Metabolism | |
Transport of MnSOD to Mitochondria | |
Muscular system | Achilles Tendinopathy Risk |
Athletes with Greater Physical Strength | |
Biceps Increase | |
Contraction of Skeletal Muscle Fibers | |
Emery-Dreifuss Muscular Dystrophy | |
Energy Spending | |
Explosive Strength | |
Fast Twitch Muscle Fibers | |
Gait Instability | |
Hand Grip Strength | |
Hard Person Syndrome | |
Increased Exercise Recovery Time | |
Increased Maximum Force Production | |
Knee strength | |
Lactate Accumulation (High Intensity Circuit) | |
Ligament Strength | |
Malignant Hyperthermia | |
Muscle Damage Protection | |
Muscle Performance | |
Muscle Performance (Angiotensin II) | |
Muscle Weakness After Exercise | |
Muscle cramps | |
Muscle growth | |
Muscle mass | |
Muscle stiffness | |
Muscle strength | |
Muscular Dystrophy – Congenital Dystroglycanopathy | |
Myostatin K153R | |
Neuromuscular Power | |
Quadriceps Muscle Strength | |
Slow-twitch fibers | |
Tendon Contractures | |
Tendon reflex | |
Transversal Physiological Area of the Quadriceps | |
Vastus Lateral Muscle | |
Neurological | Motor coordination |
Pains | Back pains |
Lumbar Disc Disease | |
Pain Sensitivity | |
Personal characteristics | Ability to Accept Criticism |
Attention deficit | |
Devotion to work | |
Higher Temperature During Exercise | |
Increased Probability of Fatigue | |
Leadership gene | |
Manual dexterity | |
Mitochondrial Energy Production | |
Morning Chronotype | |
Night chronotype | |
Resistance | |
Visuospatial Working Memory | |
Provocative | Challenging behavior |
Psychiatric | Addiction tendency (eating, gambling, alcohol, smoking) |
Disinhibition | |
Reasons for Conflict | Difficulties in Dealing with Criticism |
Respiratory system | Aerobic Resistance |
Oxygen Volume (O2) Max (VO2 Max) | |
Respiratory Quotient (RQ) | |
Skeletal system (bones) | Bone Strength |
Contracture of lower limb joints | |
Degenerative Lumbar Disc Disease | |
Elbow Flexion Contracture | |
Hip Osteoarthritis | |
Intervertebral Disc Disease | |
Musculoskeletal Pain | |
Osteoarthritis | |
Scoliosis | |
Sports | 100/200/400m race |
Ballet | |
Baseball | |
Basketball | |
Boxing | |
Climbing | |
Combat | |
Cricket | |
Cross Country | |
Cycling | |
Dance | |
Elbow flexion contracture | |
Elite athletes | |
Football (American) | |
Football (Soccer) | |
Greater Benefit of Aerobic Exercise for Vascular Function | |
Greater respiratory gains with exercise | |
Hockey | |
Improved Heart Rate with Training | |
Ironman | |
Judo | |
Karate | |
Knee flexion contracture | |
Long Distance Swimmers | |
Lung Capacity | |
MMA | |
Marathon | |
Mountain Bike | |
Muscle Damage in Low Hill Diets | |
Paragliding | |
Power Athletes | |
Race 5,000/10,000 | |
Risk Sports | |
Rowing | |
Rugby | |
Runner with more Speed than Endurance | |
Runner with more endurance than speed | |
Running Performance | |
Ski | |
Skydiving | |
Snowboard | |
Sprint | |
Surf | |
Swimming | |
Synchronized swimming | |
Tendon strength | |
Tennis | |
Trend to Exercise During Leisure | |
Triathlon | |
Triple jump | |
Volley | |
Wakeboard | |
Weightlifting | |
Windsurfing | |
Worst Motor Speed After Injury | |
Yoga | |
Vitamins | Vitamin B2 |
Vitamin B6 | |
Vitamin B9 (Folic Acid) | |
Weight | Benefit of Physical Exercise for Weight Loss |
Body fat | |
Decrease in body mass after training | |
Fat Oxidation | |
Fat burning through cycling | |
Greater Reduction in BMI with Exercise | |
Slimness |
Categories
Conditions Observed
Antioxidants / Supplements | Glutathione |
Primary Carnitine Deficiency | |
Breast cancer | Breast Neoplasm (Family) |
Breast neoplasm | |
Cancer | Colon Neoplasm |
Colorectal Neoplasm | |
Colorectal Neoplasm (Family) | |
Endometrial Neoplasm | |
Hereditary Nonpolyposis Colorectal Neoplasm | |
Ovary Neoplasm | |
Cardiovascular | Prothrombin (G20210A Mutation) |
Ventricular Tachycardia | |
Dentistry | Cleft lip |
Diabetes | Type 1 Diabetes |
Digestive system | Irritable Bowel Syndrome |
Drug Reactions | Congenital Heart Defect due to Maternal Periconception – SSRIs |
Endocrine system | Transient Neonatal Diabetes |
General | Longer Menstrual Cycle Duration |
Menstrual Migraine | |
Genetic diseases | Hereditary Breast and Ovary Cancer Syndrome |
Primary Autosomal Microcephaly | |
Primary Microcephaly | |
Hematologic system | Congenital afibrinogenemia |
Factor VII Deficiency | |
Hereditary Persistence of Fetal Hemoglobin (HPFH) | |
Hereditary diseases | Fragile X Syndrome |
Hormone | FSH deficiency |
Hormones | Aromatase Deficiency |
DHEA/DHEAS | |
Estradiol | |
Estriol | |
Estrone | |
Isolated Follicle Stimulating Hormone Deficiency (FSH) | |
Oxytocin | |
Progesterone | |
Immune system | Anti-Beta-2-Glycoprotein Antibody |
Anticardiolipin Antib. | |
Antiphospholipid Antibody Syndrome | |
Antithrombin Deficiency | |
Factor V Leiden Mutation | |
Mutation of the SERPINE1 Gene (PAI-1) | |
Phenylketonuria | |
Prolactin Promoter Polymorphism | |
Protein C Deficiency | |
Protein S Deficiency | |
Inflammations | Sjogren’s Syndrome |
Metabolic | Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency |
Weight Gain Trend | |
Methylation | MTHFR 1298 mutation (rs1801131) |
MTHFR 677 mutation (rs1801133) | |
Muscular system | Hemiplegia |
Need for Nutrients | Iron |
Pediatric | Neonatal Seizure Disorders |
Personal characteristics | Gonadal dysgenesis |
Reactions to Treatments | Allogeneic Rejection |
Reproductive system | Age at Menarche |
Endometriosis | |
Female Infertility | |
Gestational diabetes | |
In vitro fertilization | |
Infertility in Endometriosis | |
Intra-Hepatic Pregnancy Cholestasis | |
Intrauterine growth retardation | |
Male infertility | |
Neural Tube Defect | |
Organ dysfunction associated with choline deficiency | |
Ovarian Hyperstimulation Syndrome | |
Pelvic Organ Prolapse | |
Perrault Syndrome | |
Placental Detachment | |
Polycystic Ovary Syndrome | |
Pre eclampsia | |
Pregnancy | |
Pregnancy sickness | |
Premature birth | |
Risk of Recurring Pregnancy Loss | |
Spontaneous abortions | |
Uterine Fibroids | |
Uterine Fibromyoma | |
Skeletal system (bones) | Disc herniation |
Lumbopelvic Pain in Pregnancy | |
Skin | Jaundice |
Keloids | |
Varicose veins | |
Urinary system | Recurrent Urinary Infection |
Urinary incontinence | |
Vitamins | Folate |
Vitamin A | |
Vitamin B12 | |
Vitamin B6 | |
Vitamin B9 (Folic Acid) | |
Vitamin C | |
Vitamin D | |
Vitamin E | |
Vitamin K |
Categories
Conditions
Auditory system | Usher Syndrome |
Cancer | BAP1 – Tumor Predisposition Syndrome |
Retinoblastoma | |
Tumor predisposition syndrome (BAP1) | |
Diabetes | Type 1 Diabetes |
Type 2 diabetes | |
Genetic diseases | Alport’s Syndrome |
Axenfeld Rieger Syndrome | |
Blau’s Syndrome | |
Blepharophimosis Syndrome | |
Brown-Vialetto-Van Laere Syndrome | |
Elastic pseudoxanthoma | |
Joubert Syndrome | |
Mucolipidosis Type 4 (Gangliosidosis) | |
Oculocutaneous Albinism | |
Walker-Warburg Syndrome | |
Weill-Marchesani Syndrome | |
Wilson’s Disease | |
Immune system | Congenital Erythropoietic Porphyria (Gunther’s Disease) |
Graves’ Disease | |
HLA-DQ4 | |
Inflammations | Presence of the HLA-B27 Allele |
Sjogren’s Syndrome | |
Uveitis | |
Metabolic | Glycation |
Methylenetetrahydrofolate reductase (MTHFR) deficiency | |
Metabolic disorders | Homocystinuria |
Hyperferritinemia | |
Hypoalphalipoproteinemia (Tangier’s Disease) | |
Muscular system | Leigh’s Syndrome |
Muscular Dystrophy – Congenital Dystroglycanopathy | |
Need for Nutrients | Lutein |
Zeaxanthin | |
Neurodegenerative diseases | Progressive Supranuclear Palsy |
Oncologic | Choroidal Melanoma |
Personal characteristics | Double eyelids |
Reactions to Treatments | Allogeneic Rejection |
Glucocorticoid Resistance | |
Glucocorticoid Therapy | |
Skin | Basal Blade Disease |
KID Syndrome | |
Vision (Ophthalmology) | Achromatopsia |
Age Related Macular Degeneration | |
Aniridia (ophthalmus) | |
Anophthalmia | |
Astigmatism | |
Augmented S cone syndrome | |
Bradiopsia | |
Cataract | |
Choroideremia | |
Color blindness | |
Cone and Rod Dystrophy | |
Congenital Night Blindness | |
Corneal Keratometry | |
Corneal Transplant Rejection | |
Diabetic retinopathy | |
Dry Eye Syndrome | |
Early hyperopia | |
Eye color (blue) | |
Eye color (brown) | |
Eye color (brown/greenish) | |
Familial exudative vitreoretinopathy | |
Fuchs Dystrophy | |
Glaucoma | |
Glaucoma (closed angle) | |
Glaucoma (open angle) | |
Hyperopia | |
Idiopathic Polypoidal Choroid Vasculopathy | |
Keratitis | |
Keratoconus | |
Knobloch Syndrome | |
Leber’s Congenital Amaurosis | |
Leber’s Hereditary Optical Neuropathy (LHON) | |
Lentis ectopy | |
Myopia | |
Ocular Hypertension – without cupping the optic nerve | |
Oculomotor apraxia | |
Optical Density of Macular Pigments | |
Pachymetry – corneal cell count | |
Pigmentation (dark eyes) | |
Primary Congenital Glaucoma | |
Retinal detachment | |
Retinitis Pigmentosa | |
Stargardt’s Disease | |
Stickler Syndrome | |
Strabismus | |
Syndromic Microphthalmia | |
Vitelform Macular Dystrophy | |
Vitreoretinochoroidopathy | |
Zonular cataract | |
Vitamins | Beta carotene |
Categories
Conditions Observed
Aging
Aging (quality) |
Facial Age and Appearance (greater aging) |
Telomere shortening |
Allergies
Allergies in General |
Allergy to Nuts |
Allergy to Pets |
Allergy to mites |
Allergy to pollen |
Atopic Dermatitis |
Contact dermatitis |
Dermographism |
Eczema |
Mast Cell Activation Syndrome (MCAS) |
Reaction to Triclosan |
Urticaria |
Amino acids
L-arginine |
Antioxidants / Supplements
Coenzyme Q10 |
Cancer
BAP1 – Tumor Predisposition Syndrome |
Cowden’s Syndrome |
Invasive Squamous Cell Carcinoma |
Skin Neoplasm (Melanoma – Hereditary) |
Skin Neoplasm (Melanoma) |
Skin Neoplasm (light sensitivity) |
Squamous cell carcinoma |
Digestive system
Canker sores |
Fatty acids
Omega 3 |
Omega 6 |
Omega 9 |
General
Loss of hair |
Genetic diseases
Bart-Pumphrey Syndrome |
Blau’s Syndrome |
Cardio-facio-cutaneous syndrome |
Elastic pseudoxanthoma |
Hereditary angioedema |
Hypohydrotic Ectodermal Dysplasia |
Ictiosis Vulgaris |
Oculocutaneous Albinism |
Proteus Syndrome |
Hematologic system
Hyperbilirubinemia |
Post-Transfusion Purpura (PPT) |
Immune system
Congenital Erythropoietic Porphyria (Gunther’s Disease) |
Dermatomyositis |
Herpes |
Lichen Planus |
Psoriasis |
Inflammations
Behçet’s Disease |
Frontal Fibrosing Alopecia |
Sarcoidosis |
Scleroderma |
Sjogren’s Syndrome |
Metabolic
Glycation
Metabolic disorders
Acute Intermittent Porphyria |
Lipodystrophy |
Variegate Porphyria |
Microbiome
Staphylococcus aureus infections
Need for Nutrients
Apigenin need |
Turmeric (Curcumin) |
Uridine Monophosphate |
Oxidation
Antioxidant Capacity |
Oxidative stress |
Personal characteristics
Double eyelids |
Eyebrow Thickness |
Straighter hair |
Thicker hair |
Trend to Blond Hair |
Trimethylaminouria (TMAU) |
Reactions to Treatments
Glucocorticoid Resistance |
Glucocorticoid Therapy |
Skin
Acne |
Acne in Adolescence |
Alcohol Erythema Reaction |
Alopecia Areata |
Antioxidant capacity of the skin |
Armpit odor |
Atypical Mycobacteriosis |
Bags |
Baldness (Androgenetic Alopecia) |
Bulldog effect |
Cellulitis |
Ceramides |
Chicken feet |
Chin Wrinkles |
Collagen Degradation |
Collagen Synthesis |
Dark circles |
Dermatochalasis (Excess Skin on the Eyelids) |
Dystrophic Bullosa Epidermolysis |
Ehlers Danlos Syndrome (collagen) |
Elastin Deficiency |
Ephelides (Freckles) |
Erythema |
Erythropoietic Protoporphyria |
Expression Marks (Glabella) |
Eyelid sagging |
Fall from the Corner of the Mouth |
Family candidiasis |
Forehead wrinkles |
Generalized Vitiligo |
Gravitational Wrinkles |
Hereditary Chronic Mucocutaneous Candidiasis |
Hereditary Trichilemmal Cysts |
Hyaluronic acid |
Hyperchromias |
Inflammatory Skin Response |
Jaundice |
Junctional bullous epidermolysis atresia of the pylorus |
KID Syndrome |
Keloids |
Lentigos (Sun Spots) |
Leprosy |
Loss of Facial Volume |
Melasma |
Nasal wrinkles |
Nasogenian Line |
Periocular line |
Perioral Line |
Permanent Elastic Wrinkles |
Poikiloderma |
Pseudofolliculitis barbae |
Puppet Lines |
Reduced Skin Barrier Permeability Function |
Response to tanning |
Rosacea |
Sagging Neck |
Simple Bullous Epidermolysis |
Skin Aging |
Skin Hydration |
Skin Youthfulness |
Skin elasticity |
Stretch marks |
Tissue Remodeling (Healing) |
Varicose veins |
Vitiligo |
Wrinkles in the lap |
Vitamins
Vitamin A |
Vitamin B2 |
Vitamin B3 (Niacin) |
Vitamin B7 (Biotin) |
Vitamin C |
Vitamin E |
Weight
Adiposity
Categories
Conditions Observed
Cancer
Cervical Neoplasm |
Osteosarcoma |
Tumor Necrosis Factor Alpha |
Tumor calcinosis |
Dentistry
Bone resorption for prosthesis implants |
Effectiveness in response to bisphosphonates |
Digestive system
Peroxisomal Enzyme Deficiency |
Drug Reactions
Better Response to Methotrexate |
Genetic diseases
Blau’s Syndrome |
Hereditary angioedema |
Hypohydrotic Ectodermal Dysplasia |
Mucolipidosis Type 4 (Gangliosidosis) |
Seckel’s Syndrome |
Weaver syndrome |
Hematologic system
Neuroferritinopathy |
Hereditary diseases
Pompe disease |
Hormone
Acromegaly |
Growth Hormone (GH) Deficiency |
Hormones
Estradiol |
Growth Hormone Response |
Testosterone |
Immune system
Ankylosing spondylitis |
Lupus |
Lymphedema |
Psoriatic arthritis |
Inflammations
Arthrosis of the Knee |
Presence of the HLA-B27 Allele |
Sciatica |
Yao’s Syndrome |
Injuries
Fractures |
Hip dislocation |
Meniscus Injury |
Probability of Muscle Injuries |
Read – Repetitive strain injury |
Shoulder Shift |
Sports-Related Musculoskeletal Injuries |
Metabolic
Mitochondrial Complex Deficiency 1 |
Metabolic disorders
Adenosine Monophosphate Deaminase Deficiency |
Homocystinuria |
Myoadenylate Deaminase Deficiency |
Muscular system
Calf muscle hypertrophy |
Diastrophic Dysplasia |
Dissegmental Dysplasia |
Dystonia |
Emery-Dreifuss Muscular Dystrophy |
Gait Instability |
Hand Grip Strength |
Hemiplegia |
Knee strength |
Leigh’s Syndrome |
Ligament Strength |
Malignant Hyperthermia |
McArdle’s disease |
Melas Syndrome |
Muscle Damage Protection |
Muscle Hypotonia |
Muscle cramps |
Muscle stiffness |
Muscle strength |
Muscular Dystrophy – Congenital Dystroglycanopathy |
Myasthenia Grave |
Myochemy |
Myotonic dystrophy |
Nemaline myopathy |
Phosphoglycerate mutase deficiency myopathy |
Progressive Muscle Atrophy |
Progressive Muscular Dystrophy (juvenile) |
Pseudorheumatoid Dysplasia |
Refsum Disease |
Rhabdomyolysis |
Rotator Cuff Tendinitis (Tennis Shoulder) |
Spinal Muscular Atrophy |
Tendon reflex |
Vestibular Dysfunction |
Von Eulenburg Congenital Paramyotonia |
Waist Muscular Dystrophy |
X-linked Ectodermal Dysplasia |
Neurodegenerative diseases
Motor Neuropathy |
Peripheral neuropathy |
Progressive Supranuclear Palsy |
Neurological
GLUT1 Deficiency Syndrome |
Pains
Back pains |
Lumbar Disc Disease |
Pain Sensitivity |
Pediatric
Spina bifida |
Personal characteristics
Antley-Bixley Syndrome with Genital Anomaly |
Chondrodysplasia punctate rhizomelic |
Height |
Spondyloepiphyseal Dysplasia |
Skeletal system (bones)
Atelosteogenesis |
Bone mineral density |
Carpal tunnel syndrome |
Contracture of lower limb joints |
Degenerative Lumbar Disc Disease |
Disc herniation |
Dupuytren’s Contracture |
Femoral Head Avascular Necrosis |
Hip Osteoarthritis |
Intervertebral Disc Disease |
Lyme Disease (Borreliosis) |
Musculoskeletal Pain |
Osteoarthritis |
Osteogenesis Imperfecta |
Osteopenia |
Osteopetrosis |
Osteophytosis |
Osteoporosis |
Rheumatoid arthritis |
Risk of amputation in case of diabetic foot ulcer |
Scoliosis |
Skeletal Dysplasia |
Ulnar Deviation |
Sports
Elbow flexion contracture |
Knee flexion contracture |
Tendon strength |
Vision (Ophthalmology)
Knobloch Syndrome |
Leber’s Hereditary Optical Neuropathy (LHON) |
Oculomotor apraxia |
Categories
Conditions Observed
Allergies
Allergic Asthma |
Allergic Rhinitis |
Allergies in General |
Allergy to Nuts |
Allergy to Pets |
Allergy to Shrimp |
Allergy to mites |
Allergy to pollen |
Asthma |
Atopic Dermatitis |
Cockroach allergy |
Cold-induced hives |
Contact dermatitis |
Eczema |
Egg White Allergy |
Grass allergy |
Histamine Intolerance |
IgE |
Mast Cell Activation Syndrome (MCAS) |
Milk Allergy |
Peach Allergy |
Peanut Allergy |
Cancer
Thyroid Neoplasm |
Cardiovascular
Prothrombin (G20210A Mutation) |
Cardiovascular and Cerebrovascular
Phospholipase Cg2 Defect |
Cells
Autophagy |
Diabetes
Early Type 2 Diabetes |
MODY Type 1 Diabetes |
MODY Type 2 Diabetes |
MODY Type 3 Diabetes |
MODY Type 4 Diabetes |
MODY Type 5 Diabetes |
MODY Type 6 Diabetes |
MODY Type Diabetes |
Type 1 Diabetes |
Type 2 diabetes |
Digestive system
Hirschsprung’s Disease (HD) |
Permeable Intestine Syndrome |
Primary Biliary Cirrhosis (CBP) |
Ulcerative Colitis |
Endocrine system
Autoimmune Thyroid Disease |
Hashimoto’s Thyroiditis |
Hashimoto’s Thyroiditis (in children) |
Hyperparathyroidism |
Hyperthyroidism |
Hypothyroidism |
Hypothyroidism (Goiter) |
T3 |
Thyroid Orbitopathy (OT) |
Thyroid dyshormonogenesis |
Thyrotoxicosis |
Genetic diseases
Familial Amyloidotic Polyneuropathy (FAP) |
Family Mediterranean Fever |
Hereditary angioedema |
Hyperimmunoglobulin E (Hyper IgE) Syndrome |
Rasopathies |
Selective IgA Deficiency |
Hematologic system
Activated partial thromboplastin time (aPTT) |
Alpha-Defensins Levels |
Hemolytic Anemia |
High ferritin (in men) |
Post-Transfusion Purpura (PPT) |
Tendency to have Increased Eosinophils in Contact with Allergens |
Thrombophilia (Factor V – Protein C) |
Hormone
Change of Timo |
Reduction of Thyroid Hormonal Metabolism |
TSH |
Thyroid Function |
Thyroid Hormone Metabolism (T3: T4 Reduced Ratio) |
Immune system
Acquired Immune Response |
Ankylosing spondylitis |
Anti-Beta-2-Glycoprotein Antibody |
Anti-DNA Antibody |
Anticardiolipin Antib. |
Antiphospholipid Antibody Syndrome |
Antithrombin Deficiency |
Autoimmune Lymphoproliferative Syndrome (ALPS) |
B Lymphocyte Deficiency |
C3 (immune) deficiency |
Chronic Granulomatous Disease (CGD) |
Combined immunodeficiency due to magnesium deficiency (XMEN) |
Common Variable Immunodeficiency – type 1 |
Common Variable Immunodeficiency – type 2 |
Common Variable Immunodeficiency – type 8 |
Crohn’s disease |
Defect in Thyroid Hormonogenesis |
Dermatomyositis |
Factor V Leiden Mutation |
Familial hemophagocytic lymphohistiocytosis (HLH) |
Graves’ Disease |
Guillain-Barré Syndrome |
HLA-DQ2.2 |
HLA-DQ2.5 |
HLA-DQ4 |
HLA-DQ7 |
HLA-DQ8 |
Herpes |
Immunodeficiency with Hyper IgM – type 1 |
Increased Susceptibility to Contracting HIV-1 |
Lichen Planus |
Lupus |
Lupus anticoagulant |
Lymphedema |
MYD88 deficiency |
Mannose Binding Protein Deficiency |
Mutation of the SERPINE1 Gene (PAI-1) |
Myeloperoxidase Deficiency |
Neurosarcoidosis |
Polyglandular deficiency syndromes |
Primary Sclerosing Cholangitis |
Prolactin Promoter Polymorphism |
Protein C Deficiency |
Protein S Deficiency |
Psoriasis |
Psoriatic arthritis |
Risk of Decreased Metabolism of Thyroid Hormones |
Severe Combined Immunodeficiency Syndrome |
Severe Combined Immunodeficiency with Sensitivity to Ionizing Radiation |
Severe Congenital Neutropenia |
Severe Congenital Neutropenia and Cyclic Neutropenia |
T Lymphocyte Deficiency |
Type 2 X-linked Lymphoproliferative Syndrome |
Wegener’s granulomatosis |
X-Linkerd Lymphoproliferative (XLP) Syndrome |
X-linked Lymphoproliferative Syndrome (XLP) |
Inflammations
Behçet’s Disease |
Frontal Fibrosing Alopecia |
Idiopathic inflammatory myopathy |
Inflammatory Bowel Disease (IBD) |
Polymyositis |
Presence of the HLA-B27 Allele |
Sarcoidosis |
Scleroderma |
Sjogren’s Syndrome |
Metabolic
Celiac disease |
Gluten Intolerance |
Glycation |
Greater Insulin Sensitivity with Physical Exercise |
Lactose intolerance |
Metabolic disorders
Fetuin-A |
Methylation
MTHFR 1298 mutation (rs1801131) |
MTHFR 677 mutation (rs1801133) |
Muscular system
Myasthenia Grave |
Neurodegenerative diseases
Charcot-Marie Disease |
Louis-Bar Syndrome (Ataxia Telangiectasia) |
Multiple sclerosis |
Systemic Sclerosis |
Respiratory system
Chronic obstructive pulmonary disease |
Skeletal system (bones)
Arthritis |
Carpal tunnel syndrome |
Osteoarthritis |
Osteoporosis |
Rheumatoid arthritis |
Risk of amputation in case of diabetic foot ulcer |
Skin
Alopecia Areata |
Generalized Vitiligo |
Rosacea |
Vitiligo |
Urinary system
Membranoproliferative Glomerulonephritis (GNMP) |
Nephrotic syndrome |
Vision (Ophthalmology)
Diabetic retinopathy |
Categories
Conditions Observed
Cancer
Acute Lymphoblastic Leukemia (ALL) |
Childhood Acute Lymphoblastic Leukemia |
Childhood Leukemia |
Erythrocytosis |
JAK2 V617F mutation |
Myelodysplastic Syndrome |
Myeloproliferative Disorder |
Peripheral T cell lymphoma |
Polycythemia Vera |
Cardiovascular
Arginine-succinic aciduria |
Atherosclerosis (hyperlipidemia) |
Benefit of Niacin in Reducing Lipoprotein (a) |
Cardiovascular Disease (Cholesterol Level) |
Dysfunctional HDL |
Familial Hyperlipoproteinemia Type III |
Hereditary familial hypercholesterolemia |
Hypercholesterolemia (Type B) |
Jervell and Lange-Nielsen Syndrome |
Narrowing of Blood Vessels (Stenosis) |
Platelets (Highest Count) |
Platelets (Lowest Count) |
Prothrombin (G20210A Mutation) |
Pulmonary Embolism |
Venous Thromboembolism (VTE) |
Cardiovascular and Cerebrovascular
Homocysteine Accumulation |
Lipoprotein (a) |
Clopidogrel
Response to Clopidogrel |
Diabetes
Fasting Glucose Level Increase |
Digestive system
Gilbert’s Syndrome |
General
ALT / AST Index |
Genetic diseases
A1 A2 Alloantigen Polymorphism |
Alpha Antitrypsin Deficiency (AAT) |
Alpha-2-Macroglobulin Polymorphism |
Cholesterol Ester Transfer Protein Deficiency |
Elliptocytosis |
Factor II Deficiency (Prothrombin) |
Factor VII Protease Polymorphism (Marburg) |
Gamma-Glutamylcysteine Synthetase Deficiency |
Glutathione Synthetase Deficiency |
Hereditary angioedema |
Hyperimmunoglobulin E (Hyper IgE) Syndrome |
Leukocyte Adhesion Deficiency – Type 1 |
Mevalonate Kinase Deficiency |
Multiple Sulphatase Deficiency (Austin’s Disease) |
OKT4 deficiency |
Upshaw Schulman Syndrome |
Von Willebrand Disease |
Wiskott-Aldrich Syndrome |
Hematologic system
Activated partial thromboplastin time (aPTT) |
Afibrinogenemia |
Albumin |
Alpha-Defensins Levels |
Argininemia |
Aspartate Aminotransferase (AST) |
Atypical Hemolytic Uremic Syndrome (aHUS) |
Benefit of Physical Exercise for HDL |
Beta Thalassemia |
Bilirubin |
Bleeding Disorder (Platelets) |
Blood Glucose Level |
Carbamoyl Phosphate Synthetase I Deficiency |
Circulating Glycated Hemoglobin (HbA1c) |
Congenital Dyserythropoietic Anemia |
Congenital Thrombotic Thrombocytopenic Purpura |
Congenital afibrinogenemia |
Crigler-Najjar Syndrome |
D-dimers (Fibrin Degradation Products) |
Deficiency of Vitamin K-Dependent Coagulation Factors |
Essential Thrombocythemia |
Excess Calcium in Blood |
Factor V deficiency |
Factor VII Deficiency |
Factor XII Polymorphism |
Factor XIII deficiency |
Fanconi’s anemia |
G6PD deficiency |
Galactose Epimerase Deficiency |
Glanzmann’s thrombasthenia |
HDL (Cholesterol) |
HDL Deficiency (Family) |
Haptoglobin |
Hemochromatosis |
Hemolytic Anemia |
Hemophilia – Factor VIII Deficiency |
Hemophilia A |
Hemophilia B |
Hereditary Persistence of Fetal Hemoglobin (HPFH) |
Hereditary Stomatocytosis |
High Ferritin |
High ferritin (in men) |
Higher HDL on Low Carbohydrate Diets |
Hyperbilirubinemia |
Hyperhomocysteinemia |
Hypoproteinemia |
Idiopathic Hypereosinophilic Syndrome |
Intermediate Beta Thalassemia |
L-ferritin deficiency |
LDL (Cholesterol) |
Low Ferritin in Men |
Low Ferritin in Women |
Low ferritin in children under 2 years |
Lower Hemoglobin Levels |
Microcytic Anemia |
Neuroferritinopathy |
Ornithine Transcarbamylase Deficiency |
Oxidized LDL |
Paroxysmal Nocturnal Hemoglobinuria (PNH) |
Platelet Count |
Post-Transfusion Purpura (PPT) |
Reduction in Factor VIII Activity (Coagulation) |
Reduction in Factor XII Activity (Coagulation) |
Shwachman-Diamond Syndrome |
Sickle cell anemia |
Spherocytosis |
TIBC |
Tendency to have Increased Eosinophils in Contact with Allergens |
Thiamine-Responsive Megaloblastic Anemia |
Thrombocytopenia |
Thrombophilia (Factor V – Protein C) |
Thrombophilia (Factor VII) |
Transferrin |
Triglycerides |
Villejuif Hemoglobin |
X Factor Deficiency |
Hereditary diseases
Hereditary Sideroblastic Anemia |
Hormones
Hepcidin |
Immune system
Anti-Beta-2-Glycoprotein Antibody |
Anti-DNA Antibody |
Anticardiolipin Antib. |
Antiphospholipid Antibody Syndrome |
Antithrombin Deficiency |
Autoimmune Lymphoproliferative Syndrome (ALPS) |
Congenital Erythropoietic Porphyria (Gunther’s Disease) |
Factor V Leiden Mutation |
Familial hemophagocytic lymphohistiocytosis (HLH) |
Human Leukocyte Antigen (HLA) |
Lupus |
Lupus anticoagulant |
Malaria Resistance |
Mannose Binding Protein Deficiency |
Mutation of the SERPINE1 Gene (PAI-1) |
Phenylketonuria |
Primary Functional Neutrophil Disorder |
Prolactin Promoter Polymorphism |
Protein C Deficiency |
Protein S Deficiency |
Resistance to HIV (AIDS) |
Resistance to Norovirus (NoV) |
Type 2 X-linked Lymphoproliferative Syndrome |
Wegener’s granulomatosis |
X-linked Lymphoproliferative Syndrome (XLP) |
Metabolic
Ceruloplasmin |
Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency |
Greater Insulin Sensitivity with Physical Exercise |
Lactate dehydrogenase (LDH) |
Methionine Adenosyltransferase Deficiency |
Metabolic disorders
Cobalamin Intracellular Metabolism Disease |
Dyslipidemia |
Galactosemia |
Homocystinuria |
Hyperferritinemia |
Low Ferritin |
Myoadenylate Deaminase Deficiency |
Methylation
MTHFR rs1801131 |
MTHFR 1298 mutation (rs1801131) |
MTHFR 677 mutation (rs1801133) |
MTHFR rs1801133 |
Need for Nutrients
Betaine |
Iron |
Personal characteristics
Toxic Sensitivity to Benzene |
Pharmacogenetics
Warfarin |
Respiratory system
Aspergillosis |
Oxygen Volume (O2) Max (VO2 Max) |
Skin
Basal Blade Disease |
Erythropoietic Protoporphyria |
Hyperchromias |
Urinary system
Gout |
Hematuria |
Uric Acid (Concentration) |
Vitamins
Vitamin B3 (Niacin) |
Categories
Conditions Observed
Auditory system
Non-syndromic deafness |
Sudden Deafness Syndrome |
Usher Syndrome |
Breast cancer
Breast Neoplasm (Family) |
Cancer
BAP1 – Tumor Predisposition Syndrome |
Colorectal Neoplasm (Family) |
Cowden’s Syndrome |
Hereditary Cancer Predisposition Syndrome |
Hereditary Tyrosinemia Type 1 |
Li-Fraumeni Syndrome |
Lynch Syndrome |
Retinoblastoma |
Tumor predisposition syndrome (BAP1) |
Cardiovascular
Brugada Syndrome |
Familial Hyperlipoproteinemia Type III |
Familial Hypertrophic Cardiomyopathy |
Jervell and Lange-Nielsen Syndrome |
Progressive Familial Heart Block |
Romano-Ward Syndrome |
Sinus Nodule Syndrome |
Diabetes
MODY Type 3 Diabetes |
MODY Type 4 Diabetes |
MODY Type 5 Diabetes |
MODY Type 6 Diabetes |
MODY Type Diabetes |
Digestive system
Alagille Syndrome (Arteriohepatic Dysplasia) |
Congenital Lactase Deficiency |
Congenital diarrhea |
Cystic fibrosis |
Dubin-Johnson Syndrome |
Familial Intrahepatic Cholestasis |
Family diarrhea |
Irritable Bowel Syndrome |
Juvenile Polyposis Syndrome |
Trichohepatoenteric Syndrome (THE) |
Type 1 Progressive Intrahepatic Cholestasis |
Type 2 Progressive Intrahepatic Cholestasis |
Type 3 Progressive Intrahepatic Cholestasis |
Type 4 Progressive Intrahepatic Cholestasis |
General
Williams Syndrome |
Genetic diseases
Achondroplasia |
Adrenoleukodystrophy |
Alpha Antitrypsin Deficiency (AAT) |
Alpha-1 Antitrypsin Deficiency |
Alport’s Syndrome |
Angelman Syndrome |
Axenfeld Rieger Syndrome |
Bardet-Biedl Syndrome |
Berardinelli-Seip Syndrome |
Blau’s Syndrome |
Blepharophimosis Syndrome |
Bloom Syndrome |
Branched Chain Amino Acid Dehydrogenase Kinase Deficiency |
Cardio-facio-cutaneous syndrome |
Carpenter’s Syndrome |
Cat’s Eye Syndrome |
Char syndrome |
Cockayne’s Syndrome |
Cohen’s Syndrome |
Costello Syndrome |
Doors Syndrome |
Down’s syndrome |
Ellis Van Creveld Syndrome |
Epilepsy Responsive to pyridoxine |
Fabry disease |
Familial Adenomatous Polyposis |
Familial Amyloidotic Polyneuropathy (FAP) |
Familial Dysautonomy (Riley-Day Syndrome) |
Familial Glucocorticoid Deficiency (DFG) |
Familial cold autoinflammatory syndrome (FCAS) |
Familial hypobetalipoproteinemia |
Family Mediterranean Fever |
Family Periodic Fever |
HNRNPH2 |
Hereditary Breast and Ovary Cancer Syndrome |
Hereditary angioedema |
Hermansky-Pudlak Syndrome – 1 |
Hermansky-Pudlak Syndrome – 4 |
Hermansky-Pudlak Syndrome – 6 |
Hurler’s Syndrome |
Hypereplexy |
Hyperimmunoglobulin E (Hyper IgE) Syndrome |
Hyperornithinemia-Hyperammonemia-Homocitrulinuria Syndrome |
Hypohydrotic Ectodermal Dysplasia |
Joubert Syndrome |
Kabuki Syndrome |
Kindler Syndrome |
Ligase 4 Deficiency Syndrome (LIG4) |
Lucey-Driscoll Syndrome |
Maple Syrup Urine Disease (Leucinosis) |
Marfan syndrome |
Metachromatic leukodystrophy |
Miller-Dieker Syndrome |
Morquio Syndrome |
Mucolipidosis Type 4 (Gangliosidosis) |
Mucopolysaccharidosis |
Mucopolysaccharidosis Type II |
Mucopolysaccharidosis Type IIIB |
Mucopolysaccharidosis Type IVA |
Multiple Sulphatase Deficiency (Austin’s Disease) |
Noonan’s Syndrome |
PANDAS Syndrome |
PTEN Tumor Hamartoma Syndrome |
Pfeiffer’s Syndrome |
Phelan-McDermid Syndrome |
Pigment Incontinence Syndrome |
Pontocerebellar Hypoplasia |
Prader-Willi Syndrome |
Primary Hyperoxaluria |
Proteus Syndrome |
Pseudo Arisulfatase A Deficiency |
Rasopathies |
Rett Syndrome |
Salla’s disease |
Schaaf-Yang Syndrome |
Schwartz Jampel Syndrome Type 1 |
Seckel’s Syndrome |
Selective IgA Deficiency |
Smith-Lemli-Opitz Syndrome |
Smith-Magenis Syndrome |
Sotos Syndrome |
Townes Syndrome |
Transthyretin-mediated Hereditary Amyloidosis (TTR) |
Treacher-Collins Syndrome |
Tuberous Sclerosis |
Type 0B Glycogenosis |
Type 1 Gaucher Disease |
Ubiquitins |
Upshaw Schulman Syndrome |
Van der Woude Syndrome |
Walker-Warburg Syndrome |
Weaver syndrome |
Weill-Marchesani Syndrome |
Werner’s Syndrome |
Wilson’s Disease |
Wiskott-Aldrich Syndrome |
Wolfram syndrome |
Zellweger Syndrome |
Hematologic system
Afibrinogenemia |
Atypical Hemolytic Uremic Syndrome (aHUS) |
Beta Thalassemia |
Congenital Dyserythropoietic Anemia |
Fanconi’s anemia |
HDL Deficiency (Family) |
Hemochromatosis |
Hemophilia – Factor VIII Deficiency |
Hemophilia A |
Hereditary Stomatocytosis |
Intermediate Beta Thalassemia |
Sickle cell anemia |
Spherocytosis |
Thrombophilia (Factor V – Protein C) |
X-linked agammaglobulinemia |
Hereditary diseases
Fragile X Syndrome |
Friedreich’s Ataxia |
Pompe disease |
Hormones
5α-Reductase |
Aromatase Deficiency |
Immune system
Autoimmune Lymphoproliferative Syndrome (ALPS) |
Congenital Erythropoietic Porphyria (Gunther’s Disease) |
Familial hemophagocytic lymphohistiocytosis (HLH) |
Neurofibromatosis |
Severe Combined Immunodeficiency Syndrome |
Type 2 X-linked Lymphoproliferative Syndrome |
X-linked Lymphoproliferative Syndrome (XLP) |
Inflammations
Sjogren’s Syndrome |
Yao’s Syndrome |
Metabolic
Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency |
Mitochondrial Complex Deficiency 1 |
Muscular system
Becker Muscular Dystrophy |
Duchenne Muscular Dystrophy |
Emery-Dreifuss Muscular Dystrophy |
Hypotonia in Down Syndrome |
Leigh’s Syndrome |
Malignant Hyperthermia |
Melas Syndrome |
Muscular Dystrophy – Congenital Dystroglycanopathy |
Myasthenia Grave |
Neurodegenerative diseases
Becker Muscular Dystrophy |
Duchenne Muscular Dystrophy |
Emery-Dreifuss Muscular Dystrophy |
Hypotonia in Down Syndrome |
Leigh’s Syndrome |
Malignant Hyperthermia |
Melas Syndrome |
Muscular Dystrophy – Congenital Dystroglycanopathy |
Myasthenia Grave |
Neurological
Canavan disease |
Charcot-Marie Disease |
Congenital Central Hypoventilation |
Huntington’s Disease |
Louis-Bar Syndrome (Ataxia Telangiectasia) |
Pick’s Disease |
Spinocerebellar Ataxia |
Tay-Sachs disease |
Torsional dystonia |
Wolfram Syndrome-1 |
Personal characteristics
GLUT1 Deficiency Syndrome |
West syndrome |
Psychiatric
Antley-Bixley Syndrome with Genital Anomaly |
Reproductive system
Restless Legs Syndrome (Willis-Ekbom disease) |
Tourette’s Syndrome |
Skeletal system (bones)
Perrault Syndrome |
Polycystic Ovary Syndrome |
Skin
Hypochondroplasia |
Léri-Weill dyschondrosteosis |
Urinary system
Bartter’s Syndrome |
Familial Amyloid Nephropathy with Urticaria and Deafness |
Polycystic Kidney Disease (DRP) |
Renal agenesis |
Vision (Ophthalmology)
Choroideremia |
Dry Eye Syndrome |
Knobloch Syndrome |
Stickler Syndrome |
Vitamins need
Biotinidase Deficiency |
Categories
Conditions Observed
Allergies
Alcohol Aversion |
Gluten Sensitivity |
Amino acids
Glutamate Production |
L-theanine |
L-tyrosine |
Serine Deficiency |
Antioxidants / Supplements
Coenzyme Q10 |
Glutathione |
Need for a diet rich in antioxidants |
Probiotics |
Behavioral Changes
Mood Disorder |
Behaviors
Dopamine Levels |
Benefit
Chamomile |
S-adenosylmethionine (SAMe) |
Stevia Sweetener Benefit |
Cancer
Multiple Endocrine Neoplasm |
Thyroid Neoplasm |
Cardiovascular
Arginine-succinic aciduria |
Familial Hyperlipoproteinemia Type III |
Hereditary familial hypercholesterolemia |
Hypercholesterolemia (Type B) |
Cardiovascular and Cerebrovascular
Homocysteine Accumulation |
Hypertension |
Phospholipase Cg2 Defect |
Sensitivity to Salt (Hypertension) |
Diabetes
CAPN10 |
DPP-4 |
Diabetic Neuropathy |
ENPP1 |
Early Type 2 Diabetes |
Fasting Glucose Level Increase |
Fasting Insulin |
GLP-1 |
GLUT4 |
Glucose Intolerance |
IRS-1 |
Insulin Sensitivity |
Insulinogenic Index |
Lower Insulin Secretion |
MODY Type 1 Diabetes |
MODY Type 2 Diabetes |
MODY Type 3 Diabetes |
MODY Type 4 Diabetes |
MODY Type 5 Diabetes |
MODY Type 6 Diabetes |
MODY Type Diabetes |
PI3K |
Reduction in Insulin Secretion |
Regulation of Oxidative Phosphorylation in Skeletal Muscle |
Type 1 Diabetes |
Type 2 diabetes |
Weight Reduction in Liraglutide Treatment |
Β Cell Function Impairment |
Digestive system
Family diarrhea |
Hyperglycinuria |
Hyperlipoproteinemia |
Peroxisomal Enzyme Deficiency |
Drug Reactions
Better Response to Methotrexate |
Endocrine system
Addison’s Disease |
Autoimmune Thyroid Disease |
Benefit of adopting a low glycemic index diet |
Congenital Adrenal Hypoplasia (CAC) |
Hashimoto’s Thyroiditis |
Hyperparathyroidism |
Hyperthyroidism |
Hypophosphatemic Rickets |
Hypothyroidism |
Hypothyroidism (Goiter) |
Monogenic Diabetes |
Resistance to Thyroid Hormone |
Severe Neonatal Hyperparathyroidism |
T3 |
Thyroid Orbitopathy (OT) |
Thyroid dyshormonogenesis |
Thyrotoxicosis |
Transient Neonatal Diabetes |
Essential Amino Acids
L-lysine |
L-methionine |
Fatty acids
Omega 6 |
Omega 9 |
General
Alcohol Intolerance |
Aversion to Vegetables and Coffee |
GS |
INSR |
p70S6K |
Genetic diseases
Alpha Antitrypsin Deficiency (AAT) |
Alpha Hydroxyphenylpyruvate Hydroxylase Deficiency |
Chitotrioidase Deficiency |
Cholesterol Ester Transfer Protein Deficiency |
Congenital Adrenal Hyperplasia (CAC) |
Cytichrome-C Oxidase Deficiency |
Deficiency of Tetrahydrobiopterin Synthesis |
Dihydropyridine Dehydrogenase Deficiency |
Familial Adenomatous Polyposis |
Familial Glucocorticoid Deficiency (DFG) |
Gamma-Glutamylcysteine Synthetase Deficiency |
Glutathione S-transferase-1 Mutation |
Glutathione Synthetase Deficiency |
Lysosomal Acid Lipase Deficiency |
Mevalonate Kinase Deficiency |
Mutation of Glutathione Peroxidase-1 |
Mutation of Glutathione S-transferase (GST) theta 1 |
Mutation of Glutathione S-transferase M1 |
Mutation of Iodothyronine Deiodinase 2 |
Mutation of Superoxide Dismutase-1 |
Mutation of Superoxide Dismutase-2 |
Mutation of Superoxide Dismutase-3 |
OKT4 deficiency |
Platelet Glycoprotein Deficiency IV |
Pyridoxine Deficiency |
Rasopathies |
Werner’s Syndrome |
Hematologic system
Albumin |
Anemia |
Aplastic anemia |
Apolipoprotein E |
Fanconi’s anemia |
G6PD deficiency |
HDL (Cholesterol) |
HDL Deficiency (Family) |
Hemolytic Anemia |
High Ferritin |
High ferritin (in men) |
Hyperhomocysteinemia |
Hyperinsulinemia |
Hypoproteinemia |
L-ferritin deficiency |
Sickle cell anemia |
Triglycerides |
Hereditary diseases
Lipotransferase 1 deficiency |
Hormone
Acromegaly |
Adiponectin Flag |
Androstenedione |
Anti-Müllerian hormone (AMH) |
Change of Timo |
Cushing’s Syndrome |
Folic Acid Metabolism |
Growth Hormone (GH) Deficiency |
Leptin |
Luteinizing Hormone (LH) |
Reduction of Thyroid Hormonal Metabolism |
Renina’s Greatest Activity |
Resistin |
SHBG levels |
TSH |
Thyroid Function |
Thyroid Hormone Metabolism (T3: T4 Reduced Ratio) |
Hormones
5α-Reductase |
Adiponectin Levels |
Adrenal function |
Adrenaline |
Adrenocorticotrophic Hormone |
Aromatase Deficiency |
Benefit of Melatonin |
Cortisol Level |
DHEA/DHEAS |
Estradiol |
Estriol |
Estrone |
Excess of Aromatase |
Growth Hormone Response |
Impact of GH Replacement Treatment on Lipid Profile |
Increased Cortisol (in women) |
Inhibin |
Insulin Resistance |
Noradrenaline |
Parathyroid Hormone (PTH) |
Progesterone |
Somatostatin |
T4 |
Testosterone |
Vasopressin (Antidiuretic Hormone – ADH) |
Immune system
Autoimmune Disease |
C3 (immune) deficiency |
Crohn’s disease |
Defect in Thyroid Hormonogenesis |
Human Leukocyte Antigen (HLA) |
Mannose Binding Protein Deficiency |
Inflammations
Increased IL-6 with Vitamin E (Alpha-tocopherol) intake |
Sjogren’s Syndrome |
Metabolic
Ability to Digest Starch |
Ability to digest starch |
Ammonia and Glutamate Production |
BCKDK gene |
CBS Gene – Transsulfuration |
Caffeine Metabolization |
Carbohydrate Metabolism |
Decline of NAD |
Detox (Detoxification) |
Detoxification |
Glutamate to GABA Conversion |
Gluten Intolerance |
Glycation |
Greater Insulin Sensitivity with Physical Exercise |
HDL increase with Omega 6 intake |
Improving Insulin Sensitivity with Physical Exercise |
Lactate dehydrogenase (LDH) |
Leptin receptor polymorphism |
Lipid Metabolism |
Metabolic syndrome |
Methionine Adenosyltransferase Deficiency |
Methylation |
Micronutrient Metabolism |
Obesity |
Protein Metabolization |
Resting Metabolism |
Starch Metabolism |
Trend of Eating Sweets |
Trend of Overeating (Gluttony) |
Trend to regain weight |
Weight Gain Trend |
Metabolic disorders
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency |
3-Hydroxy-3-Methylglutaryl-CoA Synthetase 2 Deficiency |
3-Hydroxyacyl-CoA Dehydrogenase Deficiency |
Abetalipoproteinemia (Bassen-Kornzweig Syndrome) |
Abetalipoproteinemia (Diet) |
Adenosine Monophosphate Deaminase Deficiency |
Alpha Methyl Acetoacetic Aciduria |
Bile Acid Synthesis Deficiency |
Brain Folate Transport Deficiency |
Carnitine Acylcarnitine Translocase Deficiency |
Carnitine Palmitoyltransferase I Deficiency |
Carnitine Palmitoyltransferase II Deficiency |
Cerebral Creatine Deficiency Syndrome |
Cerebrotendinous Xanthomatosis |
Congenital Sucrase Isomaltase Deficiency |
Dopa-Responsive Dystonia (DRDSPRD) |
Dyslipidemia |
Enteropathic Acrodermatitis |
Familial hypercholanemia |
Fetuin-A |
Fructose-1,6 Bisphosphatase Deficiency |
Fructosemia |
Galactokinase Deficiency |
Galactosemia |
Glucose/Galactose Malabsorption |
Glutaric Aciduria |
Glycogen Storage Disease |
Glycogen Storage Disease Type IXa |
Glycogen Storage Disease type IXb |
Glycogenosis Type 0A |
Glycogenosis Type IB/IC |
Hereditary Folate Malabsorption |
Hereditary Fructose Intolerance |
Hyperferritinemia |
Hyperphenylalaninemia due to BH4 Deficiency |
Hyperprolinemia |
Hypophosphatasia |
It-type Congenital Glycosylation Disorder |
Lysinuric Protein Intolerance |
Lysosomal Acid Lipase Deficiency |
Maple Syrup Disease (Leucinosis) |
Medium Chain Acyl-CoA Dehydrogenase Deficiency |
Methylmalonic Acidemia |
Methylmalonic Aciduria and Homocystinuria |
Methylmalonic aciduria |
Mild Hyperphenylalaninemia without BH4 Deficiency |
Monocarboxylate Carrier 1 Deficiency |
Multiple Acyl-CoA Dehydrogenase Deficiency |
N-Acetylglutamate Synthetase Deficiency |
Niacin’s Benefit in Reducing Liver Fat |
Phosphoserine Aminotransferase Deficiency |
Pituitary Deficiency (Hypopituitarism) |
Primary Systemic Carnitine Deficiency |
Propionic Acidemia |
Purine Nucleoside Phosphorylase Deficiency |
Segawa Syndrome |
Succinyl-CoA 3-oxoacid-CoA transferase deficiency |
Thiamine 2 Metabolism Dysfunction Syndrome |
Thiamine 4 Metabolism Dysfunction Syndrome |
Thiamine 5 Metabolism Dysfunction Syndrome |
Trifunctional Mitochondrial Protein Deficiency |
Type IA glycogenosis |
Type III glycogenosis |
Type IV glycogenosis |
Type Ib Congenital Glycosylation Disorder |
Type Iz Congenital Glycosylation Disorder |
Type VI glycogenosis |
Tyrosine Hydroxylase Deficiency |
Tyrosinemia |
Very Long Chain Acyl-Coa Dehydrogenase Deficiency |
Vitamin E Deficiency |
Xenobiotic Metabolism (Including Caffeine and P-450) |
Mitochondria
Oxidative Phosphorylation |
Need for Nutrients
Apigenin need |
Benefit of Bergamot |
Betaine |
Bromelain |
Calcium |
Choline |
Chrome |
Copper |
Hop |
Iodine |
Iron |
Lutein |
Lycopene |
Magnesium |
Manganese |
Phosphatidylcholine Levels |
Phosphorus |
Potassium |
Quercetin |
Reaction to Glutamate |
Selenium |
Tetrahydrobiopterin |
Vitexin need |
Zeaxanthin |
Zinc |
Neurodegenerative diseases
Peripheral neuropathy |
Oxidation
Antioxidant Capacity |
Glutamic Acid Metabolism |
Individuals not expressing CYP3A5 |
Oxidative stress |
Personal characteristics
Alcohol Metabolism |
Greater Stimulus with Caffeine |
Hypersensitivity to Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) |
Increased Probability of Fatigue |
Mitochondrial Energy Production |
Pineal Hyperplasia |
Spondyloepiphyseal Dysplasia |
Psychiatric
Anorexia Nervosa |
Reactions to Treatments
Levothyroxine Combination therapy with Liothyronine |
Reproductive system
Age at Menarche |
Gestational diabetes |
Polycystic Ovary Syndrome |
Skeletal system (bones)
Development Defects |
Risk of amputation in case of diabetic foot ulcer |
Skin
Elastin Deficiency |
Urinary system
Uric Acid (Concentration) |
Vision (Ophthalmology)
Diabetic retinopathy |
Vitamins
Folate |
Vitamin A |
Vitamin B12 |
Vitamin B2 |
Vitamin B6 |
Vitamin B7 (Biotin) |
Vitamin B9 (Folic Acid) |
Vitamin C |
Vitamin D |
Vitamin E |
Vitamin K |
Vitamins need
Reduced Conversion of Beta Carotene to Retinol |
Riboflavin Deficiency |
Weight
Absorption of Fats |
Benefit of Physical Exercise for Weight Loss |
Fat Metabolism |
Fibers and slimming |
Ghrelin |
Greater Resistance to Weight Loss on Low Calorie Diets |
High Levels of Fatty Acids after Fat Ingestion |
Increased waist measurement with the habit of smoking a lot |
Intake of saturated fat and increased body fat |
Irisina |
Lower Use of Glucose after Carbohydrate Ingestion |
Lower Weight Gain on High Fat Diets |
Obesity (monogenic) |
Obesity in Adolescents |
Preference for bitter foods |
Preference for fatty foods |
Preference for sweet foods |
Quantitative Body Mass Index (BMI) |
Reduction of body fat with intervention of polyphenols |
Slimming with Restricted Carbohydrates Intake |
Slimness |
Trend of Higher Protein Consumption |
Trend of Monounsaturated Fat Intake and Weight Gain |
Trend of Polyunsaturated Fat Intake and Weight Gain |
Trend towards Higher Carbohydrate Consumption |
Visceral Fat Accumulation |
Waist Measure |
Waist Measurement (in Women) |
Weight Loss on Fat Reduction Diets |
Weight Loss with the Consumption of Complex Carbohydrates |
Weight Management |
Weight gain with exercise |
Weight loss and abdominal fat loss in caloric restriction |
Weight loss with more protein than carbohydrate intake |
Categories
Conditions Observed
Amino acids
N-acetylcysteine |
Cardiovascular
Long QT Syndrome |
Romano-Ward Syndrome |
Venous Thromboembolism (VTE) |
Coronavirus (COVID-19)
COVID-19-induced respiratory failure |
Coronavirus 2019 (COVID-19) |
Covid-19 protection |
Cytokine Storm |
Increased Risk of Intensive Care with Covid-19 |
Risk of severe COVID-19 |
Cytokine Storm
CCL2 (MCP-1) |
CXCL10 |
CXCR2 |
IL-1 |
IL-10 |
IL-10RB |
IL-17 |
IL-1B |
IL-6 |
IL-8 (CXCL8) |
MCP1 |
MEFV |
TGF-B |
TNFRSF1B |
VEGF |
Genes
IFN-A |
IL-1R |
IL-8 |
Hematologic system
Alpha-Defensins Levels |
Thrombocytopenia |
Immune system
CCL-3 |
CCL-5 |
IFN-γ (Interferon-Gamma) |
IFNAR1 |
IFNAR2 |
IL-12RB1 |
Need for Nutrients
Lycopene |
Magnesium |
Quercetin |
Selenium |
Zinc |
Respiratory system
Avian Influenza (H7N9) |
Flu (Influenza) |
H1N1 flu |
H3N2 – Variant of Influenza A |
Influenza B |
Pneumonia from H1N1 |
Poor Prognoses in Respiratory Disease |
Pulmonary Sepsis |
Pulmonary fibrosis |
Respiratory Syncytial Virus (RSV) |
SARS Pneumonia |
Severe Acute Respiratory Syndrome |
Tuberculosis |
Vitamins
Vitamin A |
Vitamin B1 (Thiamine) |
Vitamin B12 |
Vitamin B6 |
Vitamin B9 (Folic Acid) |
Vitamin C |
Vitamin D |
Vitamin E |
Categories
Conditions Observed
Behavioral
COMT |
Hormones
Oxytocin |
Vasopressin (Antidiuretic Hormone – ADH) |
Neurological
Dopamine Receptors |
Dopamine Synthesis |
Dopamine degradation |
Serotonin Receptors |
Serotonin Synthesis |
Serotonin degradation |
Categories
Conditions Observed
General
Aestuariispira |
Bacteroides_nordii |
Deltaproteobacteria |
EscherichiaShigella |
Klebsiella |
Klebsiella_variicola |
Lactivibrio |
Murimonas |
Paenibacillus |
Pelotomaculum |
Peptoniphilaceae |
Peptoniphilus |
Microbiome
Abiotrophy |
Acidaminococcaceae |
Acidaminococcus |
Acinetobacter |
Actinobacteria |
Actinobacteriaphylum |
Aestuariispira insulae |
Aggregatibacter |
Aggregatibacter actinomycetemcomitans |
Akkermansia |
Alistipes shahii |
Anaerofilum |
Anaerotruncus |
Anaerotruncus colihominis |
Anaerotypes |
Atopobium |
Bacilli |
Bacteroidales |
Bacteroides |
Bacteroides caccae |
Bacteroides dorei |
Bacteroides thetaiotamicron |
Bacteroidetes |
Barnesiellaceae |
Bifidobacterium |
Bifidobacterium angulatum |
Bifidobacterium catenulatum |
Blautia |
Blautia coccoides |
Blautia_glucerasea |
Blautia_stercoris |
Blautiagenus |
Burkholderiales |
Butyricicoccus Pullicaecorum |
Butyricimonas |
Butyricimonas paravirosa |
Butyricimonas paravirosa |
Butyricoccus |
Carnobacteriaceae |
Choriobacteriaceae |
Clostridium |
Clostridium IV |
Clostridium celerecrescens |
Clostridium difficile |
Clostridium xylanovorans |
Clostridium_cellulolyticum |
Clostridium_propionicum |
Coprococcus |
Coprococcus eats |
Corynebacterium Jeikeium |
Cyanobacteria |
Desulfovibrio |
Dialister |
Dialister invisus |
Dorea |
Eggerthella |
Eggerthella sinensis |
Enterobacteriaceae |
Erysipelothrix |
Erysipelotrichaceae family; Erysipelotrichales order; Erysipelotrichia class |
Erysipelotrichales |
Erysipelotrichia class, Erysipelotrichales order, Erysipelotrichaceae family |
Eubacterium |
Eubacterium Eligens |
Eubacterium ruminantium |
Euryarchaeota |
Faecalibacterium |
Faecalibacterium prausnitzii |
Firmicuts |
Fusobacterium |
Gammaproteobacteria |
Gordonibacter |
Gordonibacter pamelaeae |
Holdemania |
Klebsiella variicola |
Lachnobacterium |
Lachnospira |
Lachnospiraceae bacterium 1 1 57FAA |
Lachnospiraceae noname |
Lactivibrio alcoholicus |
Lactobacillales |
Lactobacillalesorder |
Lactobacillus |
Lactobacillus acidophilus |
Lactococcus lactis |
Lenta |
Lentisphaerae |
Leuconostoc |
Listipes |
Marinilabiliaceae |
Megamonas |
Megamonas rupelensis |
Methanobacteriaceae |
Methanobrevibacter |
Micrococcaceae |
Mogibacterium |
Murimonas intestini |
Negatives |
Oscillating |
Oscillibacter |
Peptoniphilus Asaccharolyticus |
Peptostreptococcaceae |
Phascolarctobacterium |
Phylum Proteobacteria |
Porphyromonadaceae |
Prevotelella |
Prevotella bivia |
Pseudobutyrivibrio |
Rhizobiales |
Rikenellaceae |
Rosebury |
Ruminococcus |
Ruminococcus flavefaciens |
Ruminococcus gnavus |
Ruminococcus obeum |
S_Clostridium_citroniae.chr1 |
S_Clostridium_hathewayi.chr12 |
S_Clostridium_innocuum.chr12 |
S_Clostridium_symbiosum.chr13 |
S_Lactococcus_phage_P680.chr11 |
S_Streptococcus_mutans.chr2 |
Selenomonadals |
Slackia |
Sporacetigenium |
Streptococcaceae |
Streptococcus |
Sutterellaceae |
Tenericutes |
Victivalaceae |
Victivallis |
Victivallis vadensis |
Weissella |
Xylanisolven Bacteroides |
Categories
Conditions Observed
Need for Nutrients and Metabolism
Choline |
Benefit of Turmeric (Curcumin) |
Vitamin A |
Vitamin B1 (Thiamine) |
B12 vitamin |
Absorption of Vitamin B12 (FUT2) |
Vitamin B2 |
Vitamin B3 (Niacin) |
Vitamin B5 (Pantothenic Acid) |
Vitamin B6 |
Vitamin B7 (Biotin) |
Vitamin C |
Vitamin D |
Vitamin E |
Vitamin K |
Benefit of Zeaxanthin |
Omega 3 |
Omega 6 |
Omega 9 |
Benefit of Betaine |
Benefit of Bromelain |
Calcium |
Copper |
Coenzyme Q10 |
Iron |
Phosphorus |
Selenium |
Folate |
Potassium |
Deficiency in Fat Metabolism |
Micronutrient Metabolism |
Metabolism of Xenobiotics (including caffeine and P-450) |
Caffeine Metabolization |
Benefit of Probiotics |
Lower LDL in Diets Low in Unsaturated Fats |
Iodine |
Benefit of Melatonin |
Body composition
Tendency to Depression |
Slimming with more protein intake than carbohydrates |
Weight Loss with Carbohydrate Restriction |
Weight Loss with Calorie Restriction |
Slimming with more fiber intake |
Difficulty in Maintaining Weight |
Thinning with the consumption of complex carbohydrates |
Slimming with Fat Reduction |
Preference for bitter foods |
Preference for sweet foods |
Preference for fatty foods |
Tendency to Obesity |
Tendency to Obesity (monogenic) |
Mitochondrial Energy Production |
Tendency to Anxiety |
Weight gain with saturated fat intake |
Physical activity
Physical Resistance |
Tendency to Fractures |
Aerobic Capacity |
Muscle Strength |
Muscle Mass Gain |
Runner with more endurance than speed |
Pain Tolerance |
Improved insulin sensitivity with exercise. |
Imbalances and Deficiencies
Deficiency in the Conversion of T4 to T3 |
Methylenetetrahydrofolate reductase (MTHFR) deficiency |
L-ferritin Deficiency |
Tendency to Hyperphagia |
Collagen Degradation |
Low Ferritin in Men |
Low Ferritin in Women |
Frutosemia |
Galactosemia |
Insomnia with Caffeine |
Sodium reduction to control hypertension |
Homocysteine Accumulation |
Platelet Glycoprotein Deficiency IV |
ALDH2 Deficiency |
Elastin Deficiency |
Cholesterol Level (LDL) |
Mevalonate Kinase Deficiency (MKD) |
Glucose-6-Phosphate Dehydrogenase Deficiency (G6PD) |
Growth Hormone Deficiency (GH) |
Cholesterol Level (HDL) |
Tendency to Hypertriglyceridemia |
Response to Antidepressants |
Autophagy |
Intolerances and Dysfunctions
Hypercholesterolemia (Type B) |
Hereditary Familial Hypercholesterolemia |
Hyperparathyroidism |
Hypothyroidism (Goiter) |
Type 1 Diabetes |
Type 2 Diabetes |
Early Type 2 Diabetes |
Lower Bone Mineral Density |
Cow’s Milk Allergy |
Allergy to Egg White |
Ulcerative Colitis |
Stroke |
Acute Myocardial Infarction |
Acute Myocardial Infarction (early) |
Cardiac Insufficiency |
Anorexia Nervosa |
Lactose Intolerance |
Gluten Intolerance |
Colorectal Neoplasia (Meat Consumption) |
Irritable Bowel Syndrome |
Metabolic Syndrome |
Gestational Diabetes |
Crohn’s Disease |
Gastroesophageal Reflux Disease (GERD) |
Inflammatory Bowel Disease (IBD) |
Chronic Kidney Disease (CKD) |
Autoimmune Thyroid Disease (DTA) |
Cystic Fibrosis (CF) |
Hemochromatosis |
Histamine Intolerance |
Allergy to Nuts |
Glutaric Aciduria Type I (AG1) |
Renal Tubular Acidosis (ATR) |
Abetalipoproteinemia (Bassen-Kornzweig syndrome) |
Reduction in Factor XII Activity (Coagulation) |
Attention Deficit Disorder with Food Dyes |
Non-Alcoholic Liver Steatosis |
Alzheimer’s Disease |
Parkinson’s Disease |
Ankylosing Spondylitis |
Peanut Allergy |
Alcohol Intolerance |
Glutamate Intolerance |
Mercury Intolerance |
Breast Neoplasm |
Prostate Neoplasm |
Lung Neoplasm |
Inflammation and Oxidative Stress
Need for Detoxification |
Tendency to Oxidative Stress |
IL-10 |
IL-1β |
IL-6 |
IL-8 |
IFN-γ |
TNF |
Categories
Conditions
Facial Harmonization
Collagen Degradation |
Eyelid sagging |
Neck sagging |
Nasogenian Line (Nasolabial Groove) |
Periocular Lines |
Perioral Lines |
Puppet Line |
Forehead Wrinkles |
Expression Marks (Glabela) |
Dark Circles |
Jowl |
Volume Loss and Facial Contour |
Downturned Mouth Corners |
Permanent Static Wrinkles |
Nasal Wrinkles |
Chin Wrinkles |
Gravitational Wrinkles |
Collagen Synthesis |
Hydration Capacity |
Eyelid Bags |
Skin Elasticity |
Categories
Conditions Observed
Joints
Arthrosis of the Knee |
Osteoarthritis |
Rheumatoid arthritis |
Hip Osteoarthritis |
Intestinal Inflammations
Crohn’s disease |
Inflammatory Bowel Disease (IBD) |
Ulcerative Colitis |
Leaky Bowel Syndrome |
Gluten Intolerance |
Lactose intolerance |
Respiratory
Asthma |
Rhinosinusitis |
Chronic obstructive pulmonary disease |
Skin Inflammations
Rosacea |
Atopic Dermatitis |
Contact dermatitis |
Brain Inflammation
Parkinson’s disease |
Alzheimer’s disease |
Depression |
Autoinflammatory Diseases
Blau’s Syndrome |
Family Periodic Fever |
Family Mediterranean Fever |
Familial cold autoinflammatory syndrome (FCAS) |
Behcet’s Disease |
C-reactive protein
C-reactive protein |
Pro-Inflammatory Cytokines
IL-1 |
IL-1A |
IL-1B |
IL-1R |
IL-1R2 |
IL-2 |
IL-2RA |
IL-2RB |
IL-2RG |
IL-6 |
IL-6R |
IL-7 |
IL-8 |
IL-12 |
IL-17 |
IL-17A |
IL-18 |
TNF-A |
Anti-Inflammatory Cytokines
IL-1 |
IL-4 |
IL-6 |
IL-10 |
IL-11 |
IL-13 |
IL-19 |
IL-35 |
TNF-B |
IFN-A |
IFN-G |
TGF-B |
MIP2 |
Chemokines
CCL2 |
CCL3 |
CCL5 |
CCL7 |
CCL8 |
CCL11 |
CCL13 |
CCL17 |
CCL19 |
CCL22 |
CCL25 |
CCL27 |
CCR1 |
CCR2 |
CCR3 |
CCR5 |
CXCR3 |
CXCR1 |
CCL2 |
MIP1A |
MIP1B |
MCP1 |
Hormones and Autoimmune
Testosterone |
Estradiol |
Hypothyroidism |
Cortisol Level |
Others
Rheumatic fever |
Categories
Conditions Observed
Allergies and Intolerances
Food Allergy |
Food Dye Allergy |
Peach Allergy |
Peanut Allergy |
Milk Allergy |
Allergy to Nuts and Nuts |
Allergies in General |
Histamine intolerance |
Lactose intolerance |
Gluten intolerance |
Hereditary Fructose Intolerance |
HLA-DQ2.2 |
HLA-DQ2.5 |
HLA-DQ4 |
HLA-DQ7 |
HLA-DQ8 |
Pollen Allergy |
Mite Allergy |
Asthma |
Allergic Asthma |
Reaction to Phthalate |
Reaction to Bisphenol |
Nickel Reaction |
Methylation
Methylation |
COMT |
Betaine |
B12 vitamin |
Vitamin B12 (Levels) |
Absorption of Vitamin B12 |
Vitamin B6 |
Transcobalamin II deficiency |
ACE |
MAOA |
ACAT1 |
MTR |
MTRR |
BHMT |
AHCY |
SUOX |
NOS3 |
SHMT1 |
VDR |
VDR taq rs731236 |
COMT v158m (mir4761) rs4680 |
Cellular Energy Production
Mitochondrial Energy Production |
Defect in Carnitine Transport |
Mitochondrial Biogenesis |
Primary Carnitine Deficiency |
Digestive system
Crohn’s disease |
Ulcerative Colitis |
Gastroesophageal Reflux Disease |
Inflammatory Bowel Disease (IBD) |
Celiac disease |
Antioxidants and Detoxification
Oxidative stress |
Glutathione |
Reaction to Aluminum |
Lead Reaction |
Reaction to Mercury |
Reaction to Arsenic |
Turmeric (Turmeric) |
Need for a diet rich in antioxidants |
Phase II biotransformation |
Phase I biotransformation |
Worst oxidative stress with Selenium |
SULT1A1 gene |
Detoxification |
SOD1 |
SOD2 |
SOD3 |
Detox (Detoxification) |
Folate
Vitamin B9 (Folic Acid) |
Folic Acid Metabolism |
Folate (Vitamin B9) |
MTHFR 1298 mutation (rs1801131) |
Methylenetetrahydrofolate reductase (MTHFR) deficiency |
Mutation MTHFR 677 (rs1801133) |
Methionine Cycle
L-methionine |
Methionine Adenosyltransferase Deficiency |
S-adenosylmethionine (SAMe) |
Transsulfurization Pathway
Ammonia and Glutamate Production |
CBS gene – Transsulfurization |
Neurotransmitters
Dopamine Synthesis |
Serotonin Synthesis |
Dopamine receptors |
Glutamate Production Factors |
Degradation of serotonin |
Conversion of Glutamate to GABA |
Dopamine conversion |
DRD2 |
Noradrenaline |
Tetrahydrobiopterin |
Reaction to Glutamate |
Serotonin receptors |
Urea, Nitric Oxide and BH4 Cycle
Glutathione Peroxidase-1 mutation |
Mild Hyperphenylalaninemia without BH4 Deficiency |
BH4 Deficiency Hyperphenylalaninemia |
Carbamoyl Phosphate Synthesisase Deficiency I |
Ornithine Transcarbamylase Deficiency |
Arginine-Succinic Aciduria |
Citrullinaemia |
Nitric oxide |
Argininemia |
Tetrahydrobiopterin Synthesis Deficiency |
Metabolism, hormones and detoxification.
Caffeine Metabolization |
Ubiquitins |
DHEA / DHEAS |
Fat Metabolism |
Micronutrient Metabolism |
Metabolism of Xenobiotics (including caffeine and P-450) |
Adrenal function |
Reduction of Hormonal Thyroid Metabolism |
Risk of Decreased Thyroid Hormone Metabolism |
Deficiency of Bile Acid Synthesis |
Hyperthyroidism |
Protein Metabolization |
Conversion from T4 to T3 |
Metabolism of CYP3A4 |
Adrenocorticotrophic Hormone |
Insulin resistance |
Hyperinsulinism |
Vasopressin |
Cortisol level |
Growth Hormone Deficiency (GH) |
CYP2C19 |
CYP2C19 * 1 |
CYP2C19 * 17 |
Carbohydrate Metabolism |
Vitamins and Minerals
Vitamin B5 (Pantothenic Acid) |
D vitamin |
Vitamin B1 (Thiamine) |
Anacdonic Acid Deficiency |
GcMAF protein |
Need for Vitamins |
Vitamin B7 (Biotin) |
Copper |
Vitamin E Deficiency |
Vitamin E |
Phosphatidylcholine levels |
Selenium |
Coenzyme Q10 |
Sodium |
Beta carotene |
Hemochromatosis |
Betaine |
Calcium |
Choline |
Magnesium |
Iron |
Potassium |
Vitamin A (Retinol) |
Vitamin B2 (Riboflavin) |
Zinc |
Iodine |
Hypomagnesemia |
Low Ferritin |
Molybdenum |
Phosphor |
High Ferritin |
Vitamin C |
Vitamin K |
Vitamin B3 (Niacin) |
Manganese |
Molybdenum Cofactor Deficiency |
Reduced Conversion of Beta Carotene to Retinol |
Chrome |
ASD
Autism (delayed onset of speech) |
Autism Spectrum Disorder (ASD) |
Autism (Asperger’s Syndrome) |
Autism (social communication problem) |
Growth Delay |
Motor Development Delay |
Language Disorder |
Pyroluria |
Aggressiveness in children with ADHD |
Attention Deficit Hyperactivity Disorder (ADHD) |
Hyperactivity |
Aggressiveness |
Anxiety |
Oppositional-Defiant Disorder (TOD) |
Obsessive-Compulsive Disorder (OCD) |
Dyslexia |
Attention Deficit Disorder with Food Dyes |
Social Anxiety Disorder (Social Phobia) |
Seasonal Affective Disorder (SAD) |
Bipolar Disorder (Response to Lithium Treatment) |
Bipolar disorder |
Personality Traits: Hostility, Impulsivity, Anxiety |
Challenging Behavior |
Supplementation / Pharmacogenetics
Benefit of Melatonin |
Green Tea Benefit |
Extrapyramidal Symptom with Risperidone |
Chamomile |
Bergamot Oil |
Natto benefit |
Benefit of St. John’s Wort |
Resveratrol |
Zeaxanthin |
Omega 3 |
Omega 9 |
Omega 6 |
Lutein |
Bromelain |
Quercetin |
Insomnia with Caffeine |
Reactions with the use of Antidepressants (SSRIs) |
Passionflower (Vitexin) |
Response to Fluoxetine (anti-depressant) |
Response to Hydroxychloroquine |
Anxiety with Caffeine and Insomnia |
Personal characteristics
Sense of Taste (Bitter) |
Sense of Taste (Lesser Perception of Salt) |
Sense of Taste (Sweet) |
Sense of Taste (Spicy) |
Misophony |
Aversion to Coriander |
Tendency to Overeat (Gluttony) |
Math Skills |
Obesity |
Episodic Memory |
Memory (verbal) |
Memory (long term, logic) |
Musical Aptitude |
Morning Chronotype |
Night Chronotype |
Ephelides (Freckles) |
Manual dexterity |
Osphesia |
Memory |
Visuospatial Working Memory |
Motion Sickness |
Preference for fatty foods |
Sense of Taste (Umami) |
Sense of Taste (Sour) |
Preference for sweet foods |
Preference for bitter foods |
Thinness |
Morning drowsiness |
Fragmented Sleep |
Sleep Quality |
Shortest Sleep Duration |
Sleep Disorder |
Microbiota
Clostridium |
Lactobacillus acidophilus |
Probiotics |
Family Candidiasis |
Bifidobacterium |
Lactobacillus |
Clostridium difficile |
Type of muscle fiber
Physical resistance |
Sprinter |
Endurance |
Immune system
IgE |
Hyperimmunoglobulin E Syndrome (Hyper IgE) |
C3 deficiency (immune) |
T lymphocyte deficiency |
B Lymphocyte Deficiency |
Common Variable Immunodeficiency – type 1 |
Common Variable Immunodeficiency – type 2 |
Immunodeficiency with Hyper IgM – type 1 |
Acquired Immune Response |
Eosinophilic esophagitis |
Immunodegulation, Polyiendocrinopathy and Enteropathy |
Severe Combined Immunodeficiency with Sensitivity to Ionizing Radiation |
Common Variable Immunodeficiency – type 8 |
Amino Acids
L-arginine |
L-theanine |
L-lysine |
L-tyrosine |
Serine deficiency |
Susceptibilities Diseases
Anemia |
Sickle Cell Anemia |
Hemolytic Anemia |
Microcytic Anemia |
Homocystinuria-Megaloblastic Anemia |
Thiamin-Responsive Megaloblastic Anemia |
Headache |
Biotinidase deficiency |
G6PD deficiency |
Migraine |
Phenylketonuria |
Psoriasis |
Hashimoto’s thyroiditis |
Glutathione Synthesis Deficiency |
Lyme disease (Borreliosis) |
Coronavirus 2019 (COVID-19) |
COVID-19-induced respiratory failure |
Increased Risk of Intensive Care with COVID-19 |
Risk of severe COVID-19 |
Frutosemia |
L-carnitine deficiency |
Riboflavin deficiency |
Depression in Children with Autism |
Autoimmune disease |
Autoimmune thyroid disease |
Schizophrenia |
Depression |
Astigmatism |
Myopia |
Age-Related Macular Degeneration |
Categories
Conditions Observed
Other Factors
Waist Measure |
Obesity in Adolescents |
Obesity |
Glycation |
Uric Acid (Concentration) |
Hypertension (High Blood Pressure) |
Adiponectin Levels |
C-reactive protein |
Polycystic Ovary Syndrome |
Fasting Glucose Level Increase |
Less Use of Glucose After Intake of Carbohydrates |
Quantitative Body Mass Index |
Decline of NAD |
Noradrenaline |
Leptin |
Resist |
PI3K |
AKT |
PTEN |
P70S6K |
GSK3 |
INSR |
Wolfram Syndrome 1 |
Obesity in Type 2 Diabetes Patients |
Reaction in Cells
ENPP1 |
IRS-1 |
GLUT4 |
CAPN10 |
Lipid Profile
HDL Cholesterol Level |
Cholesterol Level (LDL) |
Triglycerides |
Dyslipidemia |
Diabetes
Type 1 Diabetes |
Type 2 diabetes |
Early Type 2 Diabetes |
Insulin Resistance |
Circulating Glycated Hemoglobin (HbA1c) |
Impairment of β Cell Function |
Consequences of Diabetes
Diabetic neuropathy |
Risk of amputation in case of diabetic foot ulcer |
Diabetic retinopathy |
Increased Risk of Alzheimer’s in Diabetics (T2) |
Diabetic heart disease ischemic |
Insulin
Hyperinsulinemia |
Higher Insulin Fasting |
Hyperinsulinemic Hypoglycemia of Childhood (HHI) |
Greater Insulin Sensitivity with Physical Exercise |
Insulinogenic Index |
Insulin Sensitivity |
Lower Insulin Secretion |
Improved Insulin Resistance in Diets with More Protein |
Pharmacogenetics
Response to Metformin |
Weight Reduction in Liraglutide Treatment |
GLP-1 |
DPP-4 |
Categories
Conditions Observed
MTHFR
MTHFR rs1801131 |
MTHFR rs1801133 |
Categories
Conditions Observed
Professional
Openness to New Experiences |
Openness to new experiences (Feelings, Actions and Ideas) |
Increased Environmental Sensitivity |
Self confidence |
Ability to Solve Problems |
Challenging behavior |
Obsessive behavior |
Creativity |
Distrust |
Disinhibition |
Manual dexterity |
Difficulties in Dealing with Criticism |
Ability to Accept Criticism |
Cognitive Empathy |
Entrepreneurship |
Stress |
Extroversion |
Leadership gene |
Cognitive skills, attention and memory |
Mathematics Skill |
Impulsivity |
Intelligence – IQ |
Greater learning from mistakes |
Memory (long term, logic) |
Opportunism |
Perfectionism |
Willingness to avoid mistakes (worse red) |
Resilience |
Optimism Trend |
Decision making with greater risk |
Statistical Association with Vehicle Accidents |
Adaptive Capacity |
Self-discipline at work |
Cognitive Flexibility |
Organization |
Concern for Details |
Neurological Conditions
Morning Chronotype |
Night chronotype |
Dyslexia |
Sleep disorder |
Motion sickness |
Hyperactivity |
Early Wake Up Time |
Time to sleep later |
Insomnia |
Longer Sleep Duration (Greater Need) |
Greater Stimulus with Caffeine |
Increased Probability of Fatigue |
Memory |
Memory (traumatic) |
Memory (verbal) |
Visuospatial Working Memory |
Episodic memory |
Less Need for Sleep Hours |
Oxytocin |
Tendency to sleep late |
Type A Personality |
Type D Personality |
Neurotransmitters
Dopamine conversion |
Dopamine Synthesis |
Dopamine receptors |
Dopamine degradation |
Dopamine transporters |
Serotonin degradation |
Serotonin receptors |
Serotonin Synthesis |
Serotonin Transporters |
Behavioral Conditions
Pleasantness (Acceptability) in Men |
Pleasantness (Acceptability) in Women |
Happiness |
Musical Aptitude |
Lack of sensitivity to children |
Prosocial behavior |
Dance |
Empathy |
Fear of Uncertainties |
Lesser Sexual Desire (Female) |
Loneliness |
Shame |
Exploratory Behavior (Novelty Search) |
Migratory behavior |
Generosity |
Fears |
Sociability |
Trend of Physical Activity Practice at Leisure |
Introversion |
Psychiatric Conditions
Anorexia Nervosa |
Cataplexy and Narcolepsy (sleep) |
Depression |
Late dyskinesia |
Epilepsy |
Schizophrenia |
Risk of Depression with Parental Divorce |
Suicidal tendencies and thoughts |
Attention Deficit |
Anxiety |
Psychiatric Syndromes
Brunner Syndrome |
Panic Syndrome |
Tourette’s Syndrome |
Personality Traits
Personality Trait: Extraversion |
Personality Trait: Positive Emotions |
Personality Traits: Hostility, Impulsiveness, Anxiety |
Personality Trait: Assertiveness |
Personality Trait: Conscientiousness |
Personality Trait: Openness, Altruism, Confidence, and Modesty |
Adictions
Addition to Heroin |
Addition to Tobacco |
Alcoholism |
Cocaine addiction |
Nicotine Dependence |
Symptoms of Withdrawal in Alcoholism |
Addiction tendency (gambling, alcohol, smoking) |
Alcohol Aversion |
Emotional
Emotional Insensitivity |
Emotional Insecurity |
Emotional Maturity |
Emotional Negativity |
Emotional Vulnerability |
Relationship Difficulty |
Conflicts
Aggressiveness |
Aggression with alcohol consumption |
Antisocial behavior |
Externalizing Behavior |
Self-centeredness |
Indifference |
Neuroticism |
Anger |
Harshness |
Explosive Temperament |
Greater Tendency to Lie |
Disorders
Seasonal Affective Disorder (SAD) |
Bipolar disorder |
Social Anxiety Disorder (Social Phobia) |
Binge Eating Disorder |
Attention Deficit Hyperactivity Disorder (ADHD) |
Mood Disorder |
Internalizing Disorder |
Obsessive-Compulsive Disorder (OCD) |
Oppositional Defiant Disorder (ODD) |
Transtorno de Personalidade Borderline |
Categories
Conditions Observed
Nutrients
Omega 3 |
Omega 6 |
Hair loss
Loss of hair |
Frontal fibrous alopecia |
Congenital Universal Alopecia |
Baldness (Androgenetic Alopecia) |
Alopecia Areata |
Women Baldness |
Male Baldness |
Calvície Feminina |
Hair Features
Curly hair |
Thicker hair |
Straighter hair |
Red hair |
White Hair (Earlier Appearance) |
Pseudofoliculite |
Structure
Collagen Degradation |
Collagen Synthesis |
Ceramides |
Oxidative Stress
Oxidative stress |
Antioxidant Capacity of the Skin |
Factors of Influence
Stress |
Anxiety |
Sleep disorder |
Vitamins
Vitamin B7 (Biotin) |
Vitamin A |
Vitamin E |
Vitamin B6 |
Vitamin C |
Minerals
Copper |
Zinc |
Chrome |
Categories | Conditions Observed |
Cardio-Circulatory System | Atherosclerosis |
Hypertension (High Blood Pressure) | |
Acute myocardial infarction | |
Cholesterol Level (HDL) | |
Panel | |
Triglycerides | |
Venous Thrombosis | |
Cardiac Arrhythmia | |
High Ferritin | |
Heart disease | |
Ischemic Stroke | |
MTHFR 1298 mutation (rs1801131) | |
MTHFR 677 mutation (rs1801133) | |
Neurological System | Mental and Cognitive Decline (Age) |
Stroke | |
Alzheimer's disease | |
Parkinson's disease | |
Sleep Quality | |
Dopamine Synthesis | |
Serotonin Synthesis | |
Fertility | Male infertility |
Behavioral | Anxiety |
Seletividade em Relacionamento | |
Impulsivity | |
Fears | |
Mood Disorder | |
Depression | |
Difficulties in Receiving Reviews | |
Gastrointestinal System | Gluten Intolerance |
Lactose intolerance | |
Ulcerative Colitis | |
Leaky Gut Syndrome | |
Milk Protein Allergy | |
Irritable Bowel Syndrome | |
Ulcer | |
Celiac disease | |
Gastritis | |
Oncology | Thyroid Neoplasm |
Colorectal Neoplasm | |
Prostate Neoplasm | |
Skin Cancer | |
Lungs Cancer | |
Respiratory system | Asthma |
Flu (Influenza) | |
Bronchitis | |
Apnea | |
Pulmonary emphysema | |
Allergic Rhinitis | |
Genito-Urinary System | Kidney Calculus |
Benign Prostate Hyperplasia | |
Osteo-Muscular System | Osteoporosis |
Rheumatoid arthritis | |
Arthrosis of the Knee | |
Disc herniation | |
Endocrinological System - Disease Susceptibility | Metabolic syndrome |
Autoimmune Thyroid Disease | |
Insulin Resistance | |
Type 2 diabetes | |
Hypothyroidism | |
Endocrinological System - Hormones | Oxytocin |
Melatonin | |
Insulin | |
Cortisol | |
DHEA/DHEAS | |
Progesterone | |
Testosterone | |
Dihydrotestosterone | |
Sensory System | Cataract |
Age Related Macular Degeneration | |
Glaucoma | |
Myopia | |
Hyperopia | |
Astigmatism | |
Deafness | |
Allergies | Food Coloring Allergy |
Allergies in General |
Categories | Conditions Observed |
Immune system | MTHFR 677 mutation (rs1801133) |
MTHFR 1298 mutation (rs1801131) | |
Accumulation of Homocysteine | |
Glycation | |
Allergies in General | |
Allergy to Food Coloring | |
Cardio-Circulatory System | High Ferritin |
Atherosclerosis | |
Heart disease | |
Hypertension (High Blood Pressure) | |
Acute myocardial infarction | |
Venous Thrombosis | |
Ischemic Stroke | |
Cardiac Arrhythmia | |
Cholesterol Level (HDL) | |
Cholesterol Level (LDL) | |
Triglycerides | |
Behavioral | Depression |
Relationship Difficulty | |
Difficulties in Receiving Reviews | |
Impulsivity | |
Fears | |
Selectivity on Relationships | |
Mood Disorder | |
Anxiety | |
Oncology | Thyroid Neoplasm |
Colorectal Neoplasm | |
Breast neoplasm | |
Ovary Neoplasm | |
Endometrial Neoplasm | |
Lungs Cancer | |
Skin Cancer | |
Osteo-Muscular System | Osteoporosis |
Rheumatoid arthritis | |
Arthrosis of the Knee | |
Disc herniation | |
Genito-Urinary System | Kidney Calculus |
Candidiasis | |
Polycystic Ovary Syndrome | |
Endometriosis | |
Uterine Fibroids | |
Recurrent Urinary Tract Infection | |
Gastrointestinal System | Crohn's disease |
Lactose intolerance | |
Ulcerative Colitis | |
Leaky Gut Syndrome | |
Constipation | |
Celiac disease | |
Gluten Intolerance | |
Irritable bowel syndrome | |
Milk Protein Allergy | |
Biliary Calculations | |
Ulcer | |
Gastritis | |
Fertility | Lower Sexual Desire (Female) |
In vitro fertilization | |
Female Infertility | |
Pregnancy | |
Pregnancy sickness | |
Thyrotoxicosis | |
Recurring Gestational Loss (lower risk) | |
Intra-Hepatic Pregnancy Cholestasis | |
Uterine Fibromyoma | |
Neural Tube Defect | |
Miscarriages | |
Protein C Deficiency | |
Antithrombin Deficiency | |
Antiphospholipid Antibody Syndrome | |
Mutation of the SERPINE1 Gene (PAI-1) | |
Protein S deficiency | |
Isolated Follicle Stimulating Hormone (FSH) Deficiency | |
Fragile X Syndrome | |
FSH deficiency | |
Neurological System | Mental and Cognitive Decline (Age) |
Stroke | |
Parkinson's disease | |
Sleep Quality | |
Dopamine Synthesis | |
Serotonin Synthesis | |
Alzheimer's disease | |
Endocrinological System - Disease Susceptibility | Hypothyroidism |
Type 2 diabetes | |
Metabolic syndrome | |
Insulin Resistance | |
Hashimoto's Thyroiditis | |
Endocrinological System - Hormones | Oxytocin |
Melatonin | |
Insulin | |
Cortisol | |
DHEA/DHEAS | |
Testosterone | |
Progesterone | |
Estradiol | |
Respiratory system | Pulmonary emphysema |
Apnea | |
Asthma | |
Bronchitis | |
Flu (Influenza) | |
Allergic Rhinitis | |
Sensory System | Cataract |
Age Related Macular Degeneration | |
Glaucoma | |
Deafness | |
Myopia | |
Hyperopia | |
Astigmatism |
Categories | Conditions Observed |
Allergies | Allergic Rhinitis |
Allergies in General | |
Allergy to Pets | |
Allergy to mites | |
Allergy to pollen | |
Asthma | |
Atopic Dermatitis | |
Cockroach allergy | |
Contact dermatitis | |
Eczema | |
Egg White Allergy | |
Grass allergy | |
Histamine Intolerance | |
Milk Allergy | |
Peanut Allergy | |
Sensitivity to secondhand smoke | |
Auditory system | Non-syndromic deafness |
Otitis | |
Behavioral Changes | Aggressiveness |
Neuroticism | |
Benefits | Optimism Trend |
Cancer | Childhood Leukemia |
Retinoblastoma | |
Cardiovascular | Aortic stenosis |
Cardiac Arrhythmia | |
Cardiovascular Disease (Cholesterol Level) | |
Familial Hyperlipoproteinemia Type III | |
Hereditary familial hypercholesterolemia | |
Hypercholesterolemia (Type B) | |
Dentistry | Caries |
Periodontitis | |
Teeth development | |
Diabetes | Early Type 2 Diabetes |
Type 1 Diabetes | |
Type 2 diabetes | |
Digestive system | Canker sores |
Cystic fibrosis | |
Drug Reactions | Vaccine Reactions |
Endocrine system | Hashimoto's Thyroiditis |
Hashimoto's Thyroiditis (in children) | |
Hypothyroidism | |
General | Aversion to Vegetables and Coffee |
Bacterial Meningitis | |
Williams Syndrome | |
Genetic diseases | Angelman Syndrome |
Blepharophimosis Syndrome | |
Char syndrome | |
Cockayne's Syndrome | |
Hyperornithinemia-Hyperammonemia-Homocitrulinuria Syndrome | |
Kabuki Syndrome | |
Marfan syndrome | |
Miller-Dieker Syndrome | |
Mucopolysaccharidosis Type VI | |
PANDAS Syndrome | |
Phelan-McDermid Syndrome | |
Prader-Willi Syndrome | |
Rett Syndrome | |
Smith-Magenis Syndrome | |
Treacher-Collins Syndrome | |
Type 0B Glycogenosis | |
Ubiquitins | |
Hematologic system | Anemia |
HDL (Cholesterol) | |
Hemolytic Anemia | |
Low ferritin in children under 2 years | |
Spherocytosis | |
Triglycerides | |
Hormone | Folic Acid Metabolism |
Growth Hormone (GH) Deficiency | |
Hormones | Aromatase Deficiency |
Immune system | Allergy to Food Colors |
Chronic adenoiditis | |
HLA-DQ2.2 | |
HLA-DQ2.5 | |
HLA-DQ4 | |
HLA-DQ7 | |
HLA-DQ8 | |
Tonsillitis | |
Internalizations | Anxiety |
Depression | |
Internalizing Disorder | |
Metabolic | Celiac disease |
Lactose intolerance | |
Methylenetetrahydrofolate reductase (MTHFR) deficiency | |
Obesity | |
Trend of Eating Sweets | |
Metabolic disorders | Cerebrotendinous Xanthomatosis (CTX) |
Muscular system | Becker Muscular Dystrophy |
Dystonia | |
Need for Nutrients | Iodine |
Neurological | Motor coordination |
Rolandic Epilepsy | |
West syndrome | |
Pains | Headache |
Pediatric | Delayed Motor Development |
Neonatal Mortality | |
Personal characteristics | Attention deficit |
Circadian Rhythm Impact | |
Cognitive Flexibility | |
Cognitive empathy | |
Creativity | |
Greater Stimulus with Caffeine | |
Height | |
Hyperactivity | |
Increased Environmental Sensitivity | |
Manual dexterity | |
Memory | |
Memory (long term, logic) | |
Memory (traumatic) | |
Memory (verbal) | |
Obsessive-Compulsive Disorder (OCD) | |
Physical resistance | |
Sense of Taste (Bitter) | |
Skill in Mathematics | |
Sociability | |
Susceptibility to Bacteria | |
Tendency to sleep late | |
Visuospatial Working Memory | |
Worst Social Interaction in Autism | |
Worst Verbal Communication in Autism | |
Provocative | Oppositional defiant disorder (ODD) |
Psychiatric | Addiction tendency (eating, gambling, alcohol, smoking) |
Anorexia Nervosa | |
Attention Deficit Hyperactivity Disorder (ADHD) | |
Autism (Asperger's Syndrome) | |
Autism Spectrum Disorder (ASD) | |
Autism Visual Endophenotype | |
Cataplexy and Narcolepsy (sleep) | |
Cognitive skills, attention and memory | |
Dyslexia | |
Face Recognition Memory | |
Intelligence (higher IQ if breastfed) | |
Intelligence - IQ | |
Language disorder | |
Motion sickness | |
Non-syndromic Intellectual Disability | |
Openness to New Experiences | |
RBFOX1 gene | |
Restless Legs Syndrome (Willis-Ekbom disease) | |
Shyness | |
Type A Personality | |
Type D Personality | |
Reproductive system | Male precocious puberty |
Respiratory system | Interstitial Lung Disease |
Respiratory Syncytial Virus (RSV) | |
Skeletal system (bones) | Atelosteogenesis |
Hypochondroplasia | |
Musculoskeletal Pain | |
Scoliosis | |
Skin | Acne |
Urinary system | Chronic Kidney Disease |
Nephroliathiasis in children | |
Nephrotic syndrome | |
Renal agenesis | |
Smaller Kidneys in Newborns | |
Vision (Ophthalmology) | Astigmatism |
Myopia | |
Vitamins | Vitamin D |
Vitamins need | Biotinidase Deficiency |
Weight | Binge Eating Disorder |
Obesity in Adolescents |
Categories | Conditions Observed |
Benefit | Benefits of Coffee in Reducing the Risk of Breast Cancer |
Breast cancer | Breast Cancer Prognosis (HR+) |
Breast Neoplasm (Family) | |
Breast neoplasm | |
Ductal Carcinoma (Breast) | |
ER-positive (HR+) Breast Cancer | |
Estrogen sensitive breast cancer | |
HER2 Positive (HER2+) BC | |
PR-positive (HR+) breast cancer | |
Post-Menopause Breast Neoplasm | |
Cancer | Cervical Cancer |
Cowden's Syndrome | |
Disease Free Survival (DFS) | |
Endometrial Neoplasm | |
Higher Mammographic Density | |
Metastasis | |
Neoplasms (General Risk) | |
Ovary Neoplasm | |
Triple Negative (RH-, HER2-) | |
Triple positive (RH+, HER2+) | |
Genes | BRCA1 |
BRCA2 | |
Genetic diseases | Hereditary Breast and Ovary Cancer Syndrome |
Hormone | Adiponectin Flag |
Hormones | Aromatase Deficiency |
Progesterone | |
Oxidation | Oxidative stress |
Personal characteristics | Tendency to Larger Breasts |
Tendency to have smaller breasts | |
Reactions to Treatments | Breast Cancer risk associated with estrogen-progesterone combination therapy (EPT) |
Reproductive system | Endometriosis |
Polycystic Ovary Syndrome | |
Uterine Fibroids | |
Uterine Fibromyoma |
Categories | Conditions Observed |
Allergies | Allergic Asthma |
Allergic Rhinitis | |
Allergies in General | |
Allergy to Hydrolyzed Wheat Protein | |
Allergy to Nuts | |
Allergy to Pets | |
Allergy to Shrimp | |
Allergy to mites | |
Allergy to pollen | |
Aspirin Exacerbated Respiratory Disease (AERD) | |
Asthma | |
Atopic Dermatitis | |
Cockroach allergy | |
Cold-induced hives | |
Contact dermatitis | |
Dermographism | |
Eczema | |
Egg White Allergy | |
Grass allergy | |
Histamine Intolerance | |
IgE | |
Mast Cell Activation Syndrome (MCAS) | |
Milk Allergy | |
Peach Allergy | |
Peanut Allergy | |
Reaction to Paraben | |
Reaction to Phthalates | |
Reaction to Triclosan | |
Sensitivity to secondhand smoke | |
Cardiovascular | Sensitivity to Vehicle Pollution |
Genetic diseases | Congenital Ichthyosis |
Immune system | Allergy to Food Colors |
Food Allergy | |
Psoriasis | |
Metabolic | Celiac disease |
Gluten Intolerance | |
Lactose intolerance | |
Sensitivity to Caffeine | |
Metabolic disorders | Fructosemia |
Need for Nutrients | Quercetin |
Psychiatric | Misophony |
Motion sickness | |
Reactions to Treatments | Glucocorticoid Resistance |
Glucocorticoid Therapy | |
Respiratory system | Aspergillosis |
Rhinosinusitis | |
Skin | Alcohol Erythema Reaction |
Erythema | |
Histamine | |
Ichthyosis | |
Inflammatory Skin Response | |
Rosacea |
Categories | Conditions Observed |
Breast cancer | Ductal Carcinoma (Breast) |
Cancer | Ovary Neoplasm |
Testicular Neoplasm | |
Cardiovascular | Prothrombin (G20210A Mutation) |
Digestive system | Constipation |
Familial Intrahepatic Cholestasis | |
Drug Reactions | Congenital Heart Defect due to Maternal Periconception - SSRIs |
Reactions with the use of antidepressants (SSRI) | |
Endocrine system | Hyperthyroidism |
Thyrotoxicosis | |
Transient Neonatal Diabetes | |
General | Longer Menstrual Cycle Duration |
Menstrual Migraine | |
Hematologic system | Congenital afibrinogenemia |
Hereditary diseases | Fragile X Syndrome |
Hormone | Anti-Müllerian hormone (AMH) |
Dihydrotestosterone (DHT) | |
FSH deficiency | |
Luteinizing Hormone (LH) | |
SHBG levels | |
Hormones | Estradiol |
Inhibin | |
Isolated Follicle Stimulating Hormone Deficiency (FSH) | |
Testosterone | |
Immune system | Anti-Beta-2-Glycoprotein Antibody |
Antiphospholipid Antibody Syndrome | |
Antithrombin Deficiency | |
Defect in Thyroid Hormonogenesis | |
Factor V Leiden Mutation | |
Mutation of the SERPINE1 Gene (PAI-1) | |
Prolactin Promoter Polymorphism | |
Protein C Deficiency | |
Protein S Deficiency | |
Metabolic | Ceruloplasmin |
Methylation | MTHFR 1298 mutation (rs1801131) |
MTHFR 677 mutation (rs1801133) | |
Psychiatric | Postpartum depression |
Reproductive system | Azoospermia |
Azoospermia não obstrutiva | |
Endometriosis | |
Erectile Dysfunction | |
Erectile Dysfunction after Radiotherapy for Prostate Cancer | |
FSH levels | |
Female Infertility | |
Gestational diabetes | |
In vitro fertilization | |
Increased Excitation Levels | |
Infertility in Endometriosis | |
Intra-Hepatic Pregnancy Cholestasis | |
Male infertility | |
Male precocious puberty | |
Neural Tube Defect | |
Oligozoospermia | |
Ovarian Hyperstimulation Syndrome | |
Ovarian Response to Hormonal Stimulation | |
Pelvic Organ Prolapse | |
Peyronie's disease | |
Polycystic Ovary Syndrome | |
Pregnancy | |
Premature Ovarian Insufficiency | |
Risk of Recurring Pregnancy Loss | |
Sexual Motivation (Female) | |
Spermatocele | |
Spontaneous abortions | |
Teratozoospermia | |
Uterine Fibroids | |
Uterine Fibromyoma | |
Skeletal system (bones) | Development Defects |
Skin | Hereditary Chronic Mucocutaneous Candidiasis |
Vitamins need | Riboflavin Deficiency |
Categories | Conditions Observed |
Cancer | Oral Cavity and Laryngeal Neoplasm |
Dentistry | Aggressive Periodontitis |
Amelogenesis imperfecta (teeth) | |
Bone demineralization in the dental arch | |
Bone resorption for prosthesis implants | |
Bruxism | |
Caries | |
Dental Fluorosis | |
Dental erosion | |
Dental implant failure | |
Dentinogenesis Imperfecta | |
Duration of orthodontic treatment after premolar extraction | |
Effectiveness in response to bisphosphonates | |
Enamel hypoplasia | |
Endodontic treatment failure | |
External apical root resorption after orthodontic treatment | |
Gingivitis | |
Incisor Molar Hypomerization (HMI) | |
Increased bleeding in chronic periodontitis | |
Inflammatory and infectious endocarditis | |
Orofacial pain | |
Periodontitis | |
Persistent Apical Periodontitis | |
Pulpitis (Tooth Inflammation) | |
Resistance to demineralization of dental enamel | |
Shovel-shaped incisor teeth | |
Teeth development | |
Temporomandibular disorder | |
Third molar agenesis | |
Tooth Agenesis | |
Digestive system | Canker sores |
Genetic diseases | Van der Woude Syndrome |
Microbiome | Dialister Species |
Categories | Conditions Observed |
Amino acids | L-arginine |
Serine Deficiency | |
Antioxidants / Supplements | Coenzyme Q10 |
Retinoic Acid | |
Auditory system | Otosclerosis |
Behavioral Changes | Aggressiveness |
Cancer | Glioma |
Neuroblastoma | |
Cardiovascular | Atherosclerosis (early in children) |
Atherosclerosis (hyperlipidemia) | |
Brain aneurysm | |
Cardiovascular and Cerebrovascular | Nitric Oxide |
Stroke | |
Digestive system | Peroxisomal Enzyme Deficiency |
Fatty acids | Omega 3 |
Genetic diseases | Familial Amyloidotic Polyneuropathy (FAP) |
Familial Dysautonomy (Riley-Day Syndrome) | |
Metachromatic leukodystrophy | |
Mucopolysaccharidosis Type IIIB | |
Pseudo Arisulfatase A Deficiency | |
Salla's disease | |
Wilson's Disease | |
Zellweger Syndrome | |
Hematologic system | Argininemia |
Creatinophosphokinase | |
Neuroferritinopathy | |
Hereditary diseases | Friedreich's Ataxia |
Immune system | Guillain-Barré Syndrome |
Neurofibromatosis | |
Neurosarcoidosis | |
Inflammations | C-reactive protein |
Metabolic | Mitochondrial Complex Deficiency 1 |
Metabolic disorders | Thiamine 4 Metabolism Dysfunction Syndrome |
Muscular system | Hemiplegia |
Leigh's Syndrome | |
Need for Nutrients | Apigenin need |
Choline | |
Reaction to Glutamate | |
Turmeric (Curcumin) | |
Uridine Monophosphate | |
Neurodegenerative diseases | Alzheimer's disease |
Alzheimer's disease (early) | |
Amyotrophic Lateral Sclerosis (ALS) | |
Canavan disease | |
Cerebral Amyloid Angiopathy | |
Charcot-Marie Disease | |
Creutzfeldt-Jakob Disease | |
Delay of Alzheimer's Disease in 10 years | |
Diffuse Mesangial Sclerosis | |
Ethylmalonic Encephalopathy | |
Frontotemporal Lobar Degeneration | |
Glutaric Acidemia | |
Hereditary Sensory Neuropathy | |
Huntington's Disease | |
Louis-Bar Syndrome (Ataxia Telangiectasia) | |
Mental and Cognitive Decline (Age) | |
Molybdenum Cofactor Deficiency | |
Motor Neuropathy | |
Mucopolysaccharidosis Type IIIA | |
Multiple sclerosis | |
Neuronal Ceroid Lipofuscinosis Type 2 | |
Parkinson's disease | |
Peripheral neuropathy | |
Pick's Disease | |
Primary Progressive Aphasia | |
Progressive Supranuclear Palsy | |
Spinocerebellar Ataxia | |
Systemic Sclerosis | |
Tay-Sachs disease | |
Torsional dystonia | |
Vascular dementia (in elderly) | |
Wolfram Syndrome-1 | |
Neurological | BDNF |
Dopamine Receptors | |
Dopamine Synthesis | |
Dopamine conversion | |
Dopamine degradation | |
Dopamine transporters | |
GLUT1 Deficiency Syndrome | |
Increased Risk of Alzheimer's in Diabetics (T2) | |
Mental decline with age | |
Serotonin Receptors | |
Serotonin Synthesis | |
Serotonin Transporters | |
Serotonin degradation | |
Personal characteristics | Cognitive Flexibility |
Hypothalamus Size (Smaller GG) | |
Pineal Hyperplasia | |
Visuospatial Working Memory | |
Psychiatric | Early Wake Up Time |
Schizophrenia | |
Sleep | Time to sleep later |
Vitamins | Folate |
Vitamin B3 (Niacin) |
Categories | Conditions Observed |
Amino acids | N-acetylcysteine |
Antioxidants / Supplements | Coenzyme Q10 |
Glutathione | |
Probiotics | |
Retinol | |
Benefit | Benefit of Green Tea |
Chamomile | |
Passionflower (Vitexin) | |
S-adenosylmethionine (SAMe) | |
Cardiovascular and Cerebrovascular | Nitric Oxide |
Essential Amino Acids | L-methionine |
Fatty acids | Omega 3 |
Omega 6 | |
Omega 9 | |
Hormones | Benefit of Melatonin |
DHEA/DHEAS | |
Metabolic | Serum Ascorbate Levels |
Metabolic disorders | Hyperferritinemia |
Minerals | Blood Phosphate Levels |
Need for Nutrients | Apigenin |
Apigenin need | |
Bromelain | |
Calcium | |
Chrome | |
Copper | |
Hop | |
Iodine | |
Iron | |
Lutein | |
Lycopene | |
Magnesium | |
Manganese | |
Molybdenum | |
Phosphatidylcholine Levels | |
Phosphorus | |
Potassium | |
Quercetin | |
Resveratrol | |
Selenium | |
Uridine Monophosphate | |
Vitexin need | |
Zeaxanthin | |
Zinc | |
Vitamins | Beta carotene |
Folate | |
Inositol (Vitamin B8) | |
Nicotinamide (B3) | |
Reduction in Ascorbate Transport | |
Transcobalamin II Deficiency | |
Vitamin A | |
Vitamin B1 (Thiamine) | |
Vitamin B12 | |
Vitamin B12 (Levels) | |
Vitamin B2 | |
Vitamin B3 (Niacin) | |
Vitamin B5 (Pantothenic Acid) | |
Vitamin B6 | |
Vitamin B7 (Biotin) | |
Vitamin B9 (Folic Acid) | |
Vitamin C | |
Vitamin D | |
Vitamin E | |
Vitamin K | |
Vitamin K2 | |
Vitamins need | Riboflavin Deficiency |
Categories | Conditions Observed |
Cancer | Biliary Pathway Neoplasm |
Colorectal Neoplasm | |
Colorectal Neoplasm (Family) | |
Colorectal Neoplasm (Meat Consumption) | |
Gallbladder Neoplasm | |
Gastrointestinal Carcinoid Tumor | |
Gastrointestinal Stromal Tumor | |
Hereditary Tyrosinemia Type 1 | |
Liver Neoplasm | |
Lynch Syndrome | |
Neoplasms (General Risk) | |
Oral Cavity and Laryngeal Neoplasm | |
Pancreas Neoplasm | |
Stomach Neoplasm | |
Cardiovascular | Arginine-succinic aciduria |
Digestive system | ABCB1 Gene Polymorphisms (MDR1) |
Alagille Syndrome (Arteriohepatic Dysplasia) | |
Amyloidosis | |
Bowel polyps | |
Canker sores | |
Chronic Hepatitis (B) | |
Chronic gastritis | |
Clostridium Difficile Infection (Patients with Ulcerative Colitis) | |
Congenital Lactase Deficiency | |
Congenital diarrhea | |
Constipation | |
Cystic fibrosis | |
Dubin-Johnson Syndrome | |
Eosinophilic Esophagitis | |
Gallstones (Vesicle) | |
Gastroesophageal Reflux Disease | |
Gastroesophageal Reflux Disease | |
Gilbert's Syndrome | |
Hepatic Fibrosis | |
Hirschsprung's Disease (HD) | |
Increased Susceptibility to H. pylori Infection | |
Irritable Bowel Syndrome | |
Juvenile Polyposis Syndrome | |
Non-Alcoholic Liver Steatosis | |
Pancreatitis | |
Permeable Intestine Syndrome | |
Peroxisomal Enzyme Deficiency | |
Primary Biliary Cirrhosis (CBP) | |
Trichohepatoenteric Syndrome (THE) | |
Type 1 Progressive Intrahepatic Cholestasis | |
Type 2 Progressive Intrahepatic Cholestasis | |
Type 3 Progressive Intrahepatic Cholestasis | |
Type 4 Progressive Intrahepatic Cholestasis | |
Ulcer | |
Ulcerative Colitis | |
Drug Reactions | Hepatitis caused by anti-tuberculosis drugs |
General | ALT / AST Index |
Hepatocellular Carcinoma (HCC) | |
Protein Digestive Capacity | |
Genetic diseases | Alpha-1 Antitrypsin Deficiency |
Hereditary angioedema | |
Mucolipidosis Type 4 (Gangliosidosis) | |
Peutz-Jeghers syndrome | |
Primary Hyperoxaluria | |
Wilson's Disease | |
Zellweger Syndrome | |
Hematologic system | Albumin |
Aspartate Aminotransferase (AST) | |
Haptoglobin | |
Hemochromatosis | |
High Ferritin | |
Hyperbilirubinemia | |
Low Ferritin in Men | |
Low Ferritin in Women | |
Transferrin | |
Immune system | Crohn's disease |
HLA-DQ2.2 | |
HLA-DQ2.5 | |
HLA-DQ4 | |
HLA-DQ7 | |
HLA-DQ8 | |
Primary Sclerosing Cholangitis | |
Inflammations | Inflammatory Bowel Disease (IBD) |
Sarcoidosis | |
Yao's Syndrome | |
Metabolic | Celiac disease |
Ceruloplasmin | |
Gluten Intolerance | |
Lactose intolerance | |
Lipid Metabolism | |
Sensitivity to Caffeine | |
Metabolic disorders | Glycogen Storage Disease |
Hyperferritinemia | |
Low Ferritin | |
Methylmalonic Acidemia | |
Niacin's Benefit in Reducing Liver Fat | |
Niemann-Pick Disease | |
Need for Nutrients | Molybdenum |
Reactions to Treatments | Benefit of Aspirin on colorectal cancer risk |
Glucocorticoid Resistance | |
Glucocorticoid Therapy | |
Urinary system | Focal Segmental Glomerulosclerosis |
Risk of formation of Gallstones | |
Vitamins | Vitamin B12 (Levels) |
Weight | Binge Eating Disorder |
Reduction of body fat with intervention of polyphenols |
Categories | Conditions Observed |
Breast cancer | Breast Neoplasm (Family) |
Breast neoplasm | |
Ductal Carcinoma (Breast) | |
Cancer | Acute Lymphoblastic Leukemia (ALL) |
Adrenocortical Carcinoma | |
Astrocytoma | |
BAP1 - Tumor Predisposition Syndrome | |
Biliary Pathway Neoplasm | |
Bladder Neoplasm | |
Brain Neoplasm | |
Cervical Cancer | |
Cervical Neoplasm | |
Chordomas | |
Colon Carcinoma | |
Colorectal Neoplasm | |
Colorectal Neoplasm (Family) | |
Colorectal Neoplasm (Meat Consumption) | |
Craniopharyngioma | |
Diffuse large B-cell lymphoma | |
Endometrial Neoplasm | |
Follicular Lymphoma | |
Gallbladder Neoplasm | |
Gastrointestinal Carcinoid Tumor | |
Gastrointestinal Stromal Tumor | |
Glioma | |
Head and neck squamous cell carcinoma (HNSCC): | |
Hereditary Cancer Predisposition Syndrome | |
Hereditary Nonpolyposis Colorectal Neoplasm | |
Hereditary Tyrosinemia Type 1 | |
Hodgkin's lymphoma | |
Invasive Squamous Cell Carcinoma | |
JAK2 V617F mutation | |
Li-Fraumeni Syndrome | |
Liver Neoplasm | |
Lung Neoplasm | |
Lung adenocarcinoma | |
Lynch Syndrome | |
Malignant Pleural Mesothelioma | |
Medulloblastoma | |
Meningioma | |
Metastasis | |
Multiple Endocrine Neoplasm | |
Multiple myeloma | |
Myelodysplastic Syndrome | |
Myeloproliferative Disorder | |
Nasopharyngeal Neoplasm | |
Neoplasm: Leukemia (Blood) | |
Neoplasms (General Risk) | |
Neuroblastoma | |
Non-Hodgkin's Lymphoma | |
Non-Small Cell Lung Neoplasm | |
Oligodendroglioma | |
Oral Cavity and Laryngeal Neoplasm | |
Osteosarcoma | |
Ovary Neoplasm | |
Pancreas Neoplasm | |
Peripheral T cell lymphoma | |
Pituitary Adenoma | |
Polycythemia Vera | |
Prostate Neoplasm | |
Retinoblastoma | |
Schwannoma | |
Skin Neoplasm (Basic Cell Carcinoma - BCC) | |
Skin Neoplasm (Melanoma - Hereditary) | |
Skin Neoplasm (Melanoma) | |
Skin Neoplasm (in redheads) | |
Skin Neoplasm (light sensitivity) | |
Small Cell Lung Cancer | |
Squamous cell carcinoma | |
Stomach Neoplasm | |
Testicular Neoplasm | |
Thyroid Neoplasm | |
Tumor Carcinosis | |
Tumor Necrosis Factor Alpha | |
Tumor calcinosis | |
Tumor predisposition syndrome (BAP1) | |
Wilms' Tumor | |
Digestive system | Bowel polyps |
Juvenile Polyposis Syndrome | |
Drug Reactions | Risk of Peripheral Neuropathy using Taxane |
General | Hepatocellular Carcinoma (HCC) |
Genes | GSTT1 |
Genetic diseases | Bloom Syndrome |
Hereditary Breast and Ovary Cancer Syndrome | |
Peutz-Jeghers syndrome | |
Proteus Syndrome | |
Rasopathies | |
Hematologic system | Idiopathic Hypereosinophilic Syndrome |
Hormone | Adiponectin Flag |
Immune system | Neurofibromatosis |
Neurodegenerative diseases | Louis-Bar Syndrome (Ataxia Telangiectasia) |
Oncologic | BRAF V600E mutation |
Choroidal Melanoma | |
Reactions to Treatments | Allogeneic Rejection |
Benefit of Aspirin on colorectal cancer risk | |
Camel Milk Benefit in Smokers | |
Chemotherapy Effectiveness | |
Fluoroucacil Response | |
Glucocorticoid Resistance | |
Glucocorticoid Therapy |
Categories | Conditions Observed |
Amino acids | Beta-alanine |
L-carnitine Deficiency | |
L-glutamine | |
Monohydrate Creatine | |
Antioxidants / Supplements | BCAA levels |
Beta-Casein A1 | |
Beta-Casein A2A2 | |
Leucine Absorption | |
Retinoic Acid | |
Vegetarian Protein Shake | |
Whey Protein | |
Behaviors | Motivation to Exercise |
Persistence | |
Sports Behavior | |
Benefits | Adaptability |
Cardiovascular | Aerobic Capacity |
Brugada Syndrome | |
Cardiac Capacity | |
Familial Hypertrophic Cardiomyopathy | |
Increased blood pressure during exercise | |
Jervell and Lange-Nielsen Syndrome | |
Paroxysmal Ventricular Fibrillation | |
Romano-Ward Syndrome | |
Ventricular Tachycardia | |
Wolff-Parkinson-White Syndrome | |
Fatty acids | Arachidonic Acid Deficiency |
General | Canoeing |
Protein Digestive Capacity | |
Genetic diseases | Sudden Death Syndrome |
Walker-Warburg Syndrome | |
Hematologic system | Benefit of Physical Exercise for HDL |
High Ferritin | |
Hereditary diseases | Pompe disease |
Hormones | Cortisol Level |
DHEA/DHEAS | |
Increased Cortisol (in women) | |
Increased Noradrenaline Level During Exercise | |
Progesterone | |
Suppression of the secretion of luteinizing hormone due to anabolics | |
Testosterone | |
Injuries | Achilles tendon injury |
Anterior Cruciate Ligament Injury (ACL) | |
Best Recovery after Injury | |
Exercise Induced Muscle Damage | |
Fractures | |
Hamstring Injuries | |
Hip dislocation | |
Increased Risk of Sports Injuries | |
Ligament Rupture | |
Meniscus Injury | |
Probability of Muscle Injuries | |
Shoulder Shift | |
Sports-Related Musculoskeletal Injuries | |
Metabolic | Greater Insulin Sensitivity with Physical Exercise |
Improving Insulin Sensitivity with Physical Exercise | |
Mitochondrial Complex Deficiency 1 | |
Protein Metabolization | |
Resting Metabolic Rate | |
Resting Metabolism | |
Transport of MnSOD to Mitochondria | |
Muscular system | Achilles Tendinopathy Risk |
Athletes with Greater Physical Strength | |
Biceps Increase | |
Contraction of Skeletal Muscle Fibers | |
Emery-Dreifuss Muscular Dystrophy | |
Energy Spending | |
Explosive Strength | |
Fast Twitch Muscle Fibers | |
Gait Instability | |
Hand Grip Strength | |
Hard Person Syndrome | |
Increased Exercise Recovery Time | |
Increased Maximum Force Production | |
Knee strength | |
Lactate Accumulation (High Intensity Circuit) | |
Ligament Strength | |
Malignant Hyperthermia | |
Muscle Damage Protection | |
Muscle Performance | |
Muscle Performance (Angiotensin II) | |
Muscle Weakness After Exercise | |
Muscle cramps | |
Muscle growth | |
Muscle mass | |
Muscle stiffness | |
Muscle strength | |
Muscular Dystrophy - Congenital Dystroglycanopathy | |
Myostatin K153R | |
Neuromuscular Power | |
Quadriceps Muscle Strength | |
Slow-twitch fibers | |
Tendon Contractures | |
Tendon reflex | |
Transversal Physiological Area of the Quadriceps | |
Vastus Lateral Muscle | |
Neurological | Motor coordination |
Pains | Back pains |
Lumbar Disc Disease | |
Pain Sensitivity | |
Personal characteristics | Ability to Accept Criticism |
Attention deficit | |
Devotion to work | |
Higher Temperature During Exercise | |
Increased Probability of Fatigue | |
Leadership gene | |
Manual dexterity | |
Mitochondrial Energy Production | |
Morning Chronotype | |
Night chronotype | |
Resistance | |
Visuospatial Working Memory | |
Provocative | Challenging behavior |
Psychiatric | Addiction tendency (eating, gambling, alcohol, smoking) |
Disinhibition | |
Reasons for Conflict | Difficulties in Dealing with Criticism |
Respiratory system | Aerobic Resistance |
Oxygen Volume (O2) Max (VO2 Max) | |
Respiratory Quotient (RQ) | |
Skeletal system (bones) | Bone Strength |
Contracture of lower limb joints | |
Degenerative Lumbar Disc Disease | |
Elbow Flexion Contracture | |
Hip Osteoarthritis | |
Intervertebral Disc Disease | |
Musculoskeletal Pain | |
Osteoarthritis | |
Scoliosis | |
Sports | 100/200/400m race |
Ballet | |
Baseball | |
Basketball | |
Boxing | |
Climbing | |
Combat | |
Cricket | |
Cross Country | |
Cycling | |
Dance | |
Elbow flexion contracture | |
Elite athletes | |
Football (American) | |
Football (Soccer) | |
Greater Benefit of Aerobic Exercise for Vascular Function | |
Greater respiratory gains with exercise | |
Hockey | |
Improved Heart Rate with Training | |
Ironman | |
Judo | |
Karate | |
Knee flexion contracture | |
Long Distance Swimmers | |
Lung Capacity | |
MMA | |
Marathon | |
Mountain Bike | |
Muscle Damage in Low Hill Diets | |
Paragliding | |
Power Athletes | |
Race 5,000/10,000 | |
Risk Sports | |
Rowing | |
Rugby | |
Runner with more Speed than Endurance | |
Runner with more endurance than speed | |
Running Performance | |
Ski | |
Skydiving | |
Snowboard | |
Sprint | |
Surf | |
Swimming | |
Synchronized swimming | |
Tendon strength | |
Tennis | |
Trend to Exercise During Leisure | |
Triathlon | |
Triple jump | |
Volley | |
Wakeboard | |
Weightlifting | |
Windsurfing | |
Worst Motor Speed After Injury | |
Yoga | |
Vitamins | Vitamin B2 |
Vitamin B6 | |
Vitamin B9 (Folic Acid) | |
Weight | Benefit of Physical Exercise for Weight Loss |
Body fat | |
Decrease in body mass after training | |
Fat Oxidation | |
Fat burning through cycling | |
Greater Reduction in BMI with Exercise | |
Slimness |
Categories | Conditions Observed |
Antioxidants / Supplements | Glutathione |
Primary Carnitine Deficiency | |
Breast cancer | Breast Neoplasm (Family) |
Breast neoplasm | |
Cancer | Colon Neoplasm |
Colorectal Neoplasm | |
Colorectal Neoplasm (Family) | |
Endometrial Neoplasm | |
Hereditary Nonpolyposis Colorectal Neoplasm | |
Ovary Neoplasm | |
Cardiovascular | Prothrombin (G20210A Mutation) |
Ventricular Tachycardia | |
Dentistry | Cleft lip |
Diabetes | Type 1 Diabetes |
Digestive system | Irritable Bowel Syndrome |
Drug Reactions | Congenital Heart Defect due to Maternal Periconception - SSRIs |
Endocrine system | Transient Neonatal Diabetes |
General | Longer Menstrual Cycle Duration |
Menstrual Migraine | |
Genetic diseases | Hereditary Breast and Ovary Cancer Syndrome |
Primary Autosomal Microcephaly | |
Primary Microcephaly | |
Hematologic system | Congenital afibrinogenemia |
Factor VII Deficiency | |
Hereditary Persistence of Fetal Hemoglobin (HPFH) | |
Hereditary diseases | Fragile X Syndrome |
Hormone | FSH deficiency |
Hormones | Aromatase Deficiency |
DHEA/DHEAS | |
Estradiol | |
Estriol | |
Estrone | |
Isolated Follicle Stimulating Hormone Deficiency (FSH) | |
Oxytocin | |
Progesterone | |
Immune system | Anti-Beta-2-Glycoprotein Antibody |
Anticardiolipin Antib. | |
Antiphospholipid Antibody Syndrome | |
Antithrombin Deficiency | |
Factor V Leiden Mutation | |
Mutation of the SERPINE1 Gene (PAI-1) | |
Phenylketonuria | |
Prolactin Promoter Polymorphism | |
Protein C Deficiency | |
Protein S Deficiency | |
Inflammations | Sjogren's Syndrome |
Metabolic | Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency |
Weight Gain Trend | |
Methylation | MTHFR 1298 mutation (rs1801131) |
MTHFR 677 mutation (rs1801133) | |
Muscular system | Hemiplegia |
Need for Nutrients | Iron |
Pediatric | Neonatal Seizure Disorders |
Personal characteristics | Gonadal dysgenesis |
Reactions to Treatments | Allogeneic Rejection |
Reproductive system | Age at Menarche |
Endometriosis | |
Female Infertility | |
Gestational diabetes | |
In vitro fertilization | |
Infertility in Endometriosis | |
Intra-Hepatic Pregnancy Cholestasis | |
Intrauterine growth retardation | |
Male infertility | |
Neural Tube Defect | |
Organ dysfunction associated with choline deficiency | |
Ovarian Hyperstimulation Syndrome | |
Pelvic Organ Prolapse | |
Perrault Syndrome | |
Placental Detachment | |
Polycystic Ovary Syndrome | |
Pre eclampsia | |
Pregnancy | |
Pregnancy sickness | |
Premature birth | |
Risk of Recurring Pregnancy Loss | |
Spontaneous abortions | |
Uterine Fibroids | |
Uterine Fibromyoma | |
Skeletal system (bones) | Disc herniation |
Lumbopelvic Pain in Pregnancy | |
Skin | Jaundice |
Keloids | |
Varicose veins | |
Urinary system | Recurrent Urinary Infection |
Urinary incontinence | |
Vitamins | Folate |
Vitamin A | |
Vitamin B12 | |
Vitamin B6 | |
Vitamin B9 (Folic Acid) | |
Vitamin C | |
Vitamin D | |
Vitamin E | |
Vitamin K |
Categories | Conditions Observed |
Auditory system | Usher Syndrome |
Cancer | BAP1 - Tumor Predisposition Syndrome |
Retinoblastoma | |
Tumor predisposition syndrome (BAP1) | |
Diabetes | Type 1 Diabetes |
Type 2 diabetes | |
Genetic diseases | Alport's Syndrome |
Axenfeld Rieger Syndrome | |
Blau's Syndrome | |
Blepharophimosis Syndrome | |
Brown-Vialetto-Van Laere Syndrome | |
Elastic pseudoxanthoma | |
Joubert Syndrome | |
Mucolipidosis Type 4 (Gangliosidosis) | |
Oculocutaneous Albinism | |
Walker-Warburg Syndrome | |
Weill-Marchesani Syndrome | |
Wilson's Disease | |
Immune system | Congenital Erythropoietic Porphyria (Gunther's Disease) |
Graves' Disease | |
HLA-DQ4 | |
Inflammations | Presence of the HLA-B27 Allele |
Sjogren's Syndrome | |
Uveitis | |
Metabolic | Glycation |
Methylenetetrahydrofolate reductase (MTHFR) deficiency | |
Metabolic disorders | Homocystinuria |
Hyperferritinemia | |
Hypoalphalipoproteinemia (Tangier's Disease) | |
Muscular system | Leigh's Syndrome |
Muscular Dystrophy - Congenital Dystroglycanopathy | |
Need for Nutrients | Lutein |
Zeaxanthin | |
Neurodegenerative diseases | Progressive Supranuclear Palsy |
Oncologic | Choroidal Melanoma |
Personal characteristics | Double eyelids |
Reactions to Treatments | Allogeneic Rejection |
Glucocorticoid Resistance | |
Glucocorticoid Therapy | |
Skin | Basal Blade Disease |
KID Syndrome | |
Vision (Ophthalmology) | Achromatopsia |
Age Related Macular Degeneration | |
Aniridia (ophthalmus) | |
Anophthalmia | |
Astigmatism | |
Augmented S cone syndrome | |
Bradiopsia | |
Cataract | |
Choroideremia | |
Color blindness | |
Cone and Rod Dystrophy | |
Congenital Night Blindness | |
Corneal Keratometry | |
Corneal Transplant Rejection | |
Diabetic retinopathy | |
Dry Eye Syndrome | |
Early hyperopia | |
Eye color (blue) | |
Eye color (brown) | |
Eye color (brown/greenish) | |
Familial exudative vitreoretinopathy | |
Fuchs Dystrophy | |
Glaucoma | |
Glaucoma (closed angle) | |
Glaucoma (open angle) | |
Hyperopia | |
Idiopathic Polypoidal Choroid Vasculopathy | |
Keratitis | |
Keratoconus | |
Knobloch Syndrome | |
Leber's Congenital Amaurosis | |
Leber's Hereditary Optical Neuropathy (LHON) | |
Lentis ectopy | |
Myopia | |
Ocular Hypertension - without cupping the optic nerve | |
Oculomotor apraxia | |
Optical Density of Macular Pigments | |
Pachymetry - corneal cell count | |
Pigmentation (dark eyes) | |
Primary Congenital Glaucoma | |
Retinal detachment | |
Retinitis Pigmentosa | |
Stargardt's Disease | |
Stickler Syndrome | |
Strabismus | |
Syndromic Microphthalmia | |
Vitelform Macular Dystrophy | |
Vitreoretinochoroidopathy | |
Zonular cataract | |
Vitamins | Beta carotene |
Categories | Conditions Observed |
Aging | Aging (quality) |
Facial Age and Appearance (greater aging) | |
Telomere shortening | |
Allergies | Allergies in General |
Allergy to Nuts | |
Allergy to Pets | |
Allergy to mites | |
Allergy to pollen | |
Atopic Dermatitis | |
Contact dermatitis | |
Dermographism | |
Eczema | |
Mast Cell Activation Syndrome (MCAS) | |
Reaction to Triclosan | |
Urticaria | |
Amino acids | L-arginine |
Antioxidants / Supplements | Coenzyme Q10 |
Cancer | BAP1 - Tumor Predisposition Syndrome |
Cowden's Syndrome | |
Invasive Squamous Cell Carcinoma | |
Skin Neoplasm (Melanoma - Hereditary) | |
Skin Neoplasm (Melanoma) | |
Skin Neoplasm (light sensitivity) | |
Squamous cell carcinoma | |
Digestive system | Canker sores |
Fatty acids | Omega 3 |
Omega 6 | |
Omega 9 | |
General | Loss of hair |
Genetic diseases | Bart-Pumphrey Syndrome |
Blau's Syndrome | |
Cardio-facio-cutaneous syndrome | |
Elastic pseudoxanthoma | |
Hereditary angioedema | |
Hypohydrotic Ectodermal Dysplasia | |
Ictiosis Vulgaris | |
Oculocutaneous Albinism | |
Proteus Syndrome | |
Hematologic system | Hyperbilirubinemia |
Post-Transfusion Purpura (PPT) | |
Immune system | Congenital Erythropoietic Porphyria (Gunther's Disease) |
Dermatomyositis | |
Herpes | |
Lichen Planus | |
Psoriasis | |
Inflammations | Behçet's Disease |
Frontal Fibrosing Alopecia | |
Sarcoidosis | |
Scleroderma | |
Sjogren's Syndrome | |
Metabolic | Glycation |
Metabolic disorders | Acute Intermittent Porphyria |
Lipodystrophy | |
Variegate Porphyria | |
Microbiome | Staphylococcus aureus infections |
Need for Nutrients | Apigenin need |
Turmeric (Curcumin) | |
Uridine Monophosphate | |
Oxidation | Antioxidant Capacity |
Oxidative stress | |
Personal characteristics | Double eyelids |
Eyebrow Thickness | |
Straighter hair | |
Thicker hair | |
Trend to Blond Hair | |
Trimethylaminouria (TMAU) | |
Reactions to Treatments | Glucocorticoid Resistance |
Glucocorticoid Therapy | |
Skin | Acne |
Acne in Adolescence | |
Alcohol Erythema Reaction | |
Alopecia Areata | |
Antioxidant capacity of the skin | |
Armpit odor | |
Atypical Mycobacteriosis | |
Bags | |
Baldness (Androgenetic Alopecia) | |
Bulldog effect | |
Cellulitis | |
Ceramides | |
Chicken feet | |
Chin Wrinkles | |
Collagen Degradation | |
Collagen Synthesis | |
Dark circles | |
Dermatochalasis (Excess Skin on the Eyelids) | |
Dystrophic Bullosa Epidermolysis | |
Ehlers Danlos Syndrome (collagen) | |
Elastin Deficiency | |
Ephelides (Freckles) | |
Erythema | |
Erythropoietic Protoporphyria | |
Expression Marks (Glabella) | |
Eyelid sagging | |
Fall from the Corner of the Mouth | |
Family candidiasis | |
Forehead wrinkles | |
Generalized Vitiligo | |
Gravitational Wrinkles | |
Hereditary Chronic Mucocutaneous Candidiasis | |
Hereditary Trichilemmal Cysts | |
Hyaluronic acid | |
Hyperchromias | |
Inflammatory Skin Response | |
Jaundice | |
Junctional bullous epidermolysis atresia of the pylorus | |
KID Syndrome | |
Keloids | |
Lentigos (Sun Spots) | |
Leprosy | |
Loss of Facial Volume | |
Melasma | |
Nasal wrinkles | |
Nasogenian Line | |
Periocular line | |
Perioral Line | |
Permanent Elastic Wrinkles | |
Poikiloderma | |
Pseudofolliculitis barbae | |
Puppet Lines | |
Reduced Skin Barrier Permeability Function | |
Response to tanning | |
Rosacea | |
Sagging Neck | |
Simple Bullous Epidermolysis | |
Skin Aging | |
Skin Hydration | |
Skin Youthfulness | |
Skin elasticity | |
Stretch marks | |
Tissue Remodeling (Healing) | |
Varicose veins | |
Vitiligo | |
Wrinkles in the lap | |
Vitamins | Vitamin A |
Vitamin B2 | |
Vitamin B3 (Niacin) | |
Vitamin B7 (Biotin) | |
Vitamin C | |
Vitamin E | |
Weight | Adiposity |
Categories | Conditions Observed |
Cancer | Cervical Neoplasm |
Osteosarcoma | |
Tumor Necrosis Factor Alpha | |
Tumor calcinosis | |
Dentistry | Bone resorption for prosthesis implants |
Effectiveness in response to bisphosphonates | |
Digestive system | Peroxisomal Enzyme Deficiency |
Drug Reactions | Better Response to Methotrexate |
Genetic diseases | Blau's Syndrome |
Hereditary angioedema | |
Hypohydrotic Ectodermal Dysplasia | |
Mucolipidosis Type 4 (Gangliosidosis) | |
Seckel's Syndrome | |
Weaver syndrome | |
Hematologic system | Neuroferritinopathy |
Hereditary diseases | Pompe disease |
Hormone | Acromegaly |
Growth Hormone (GH) Deficiency | |
Hormones | Estradiol |
Growth Hormone Response | |
Testosterone | |
Immune system | Ankylosing spondylitis |
Lupus | |
Lymphedema | |
Psoriatic arthritis | |
Inflammations | Arthrosis of the Knee |
Presence of the HLA-B27 Allele | |
Sciatica | |
Yao's Syndrome | |
Injuries | Fractures |
Hip dislocation | |
Meniscus Injury | |
Probability of Muscle Injuries | |
Read - Repetitive strain injury | |
Shoulder Shift | |
Sports-Related Musculoskeletal Injuries | |
Metabolic | Mitochondrial Complex Deficiency 1 |
Metabolic disorders | Adenosine Monophosphate Deaminase Deficiency |
Homocystinuria | |
Myoadenylate Deaminase Deficiency | |
Muscular system | Calf muscle hypertrophy |
Diastrophic Dysplasia | |
Dissegmental Dysplasia | |
Dystonia | |
Emery-Dreifuss Muscular Dystrophy | |
Gait Instability | |
Hand Grip Strength | |
Hemiplegia | |
Knee strength | |
Leigh's Syndrome | |
Ligament Strength | |
Malignant Hyperthermia | |
McArdle's disease | |
Melas Syndrome | |
Muscle Damage Protection | |
Muscle Hypotonia | |
Muscle cramps | |
Muscle stiffness | |
Muscle strength | |
Muscular Dystrophy - Congenital Dystroglycanopathy | |
Myasthenia Grave | |
Myochemy | |
Myotonic dystrophy | |
Nemaline myopathy | |
Phosphoglycerate mutase deficiency myopathy | |
Progressive Muscle Atrophy | |
Progressive Muscular Dystrophy (juvenile) | |
Pseudorheumatoid Dysplasia | |
Refsum Disease | |
Rhabdomyolysis | |
Rotator Cuff Tendinitis (Tennis Shoulder) | |
Spinal Muscular Atrophy | |
Tendon reflex | |
Vestibular Dysfunction | |
Von Eulenburg Congenital Paramyotonia | |
Waist Muscular Dystrophy | |
X-linked Ectodermal Dysplasia | |
Neurodegenerative diseases | Motor Neuropathy |
Peripheral neuropathy | |
Progressive Supranuclear Palsy | |
Neurological | GLUT1 Deficiency Syndrome |
Pains | Back pains |
Lumbar Disc Disease | |
Pain Sensitivity | |
Pediatric | Spina bifida |
Personal characteristics | Antley-Bixley Syndrome with Genital Anomaly |
Chondrodysplasia punctate rhizomelic | |
Height | |
Spondyloepiphyseal Dysplasia | |
Skeletal system (bones) | Atelosteogenesis |
Bone mineral density | |
Carpal tunnel syndrome | |
Contracture of lower limb joints | |
Degenerative Lumbar Disc Disease | |
Disc herniation | |
Dupuytren's Contracture | |
Femoral Head Avascular Necrosis | |
Hip Osteoarthritis | |
Intervertebral Disc Disease | |
Lyme Disease (Borreliosis) | |
Musculoskeletal Pain | |
Osteoarthritis | |
Osteogenesis Imperfecta | |
Osteopenia | |
Osteopetrosis | |
Osteophytosis | |
Osteoporosis | |
Rheumatoid arthritis | |
Risk of amputation in case of diabetic foot ulcer | |
Scoliosis | |
Skeletal Dysplasia | |
Ulnar Deviation | |
Sports | Elbow flexion contracture |
Knee flexion contracture | |
Tendon strength | |
Vision (Ophthalmology) | Knobloch Syndrome |
Leber's Hereditary Optical Neuropathy (LHON) | |
Oculomotor apraxia |
Categories | Conditions Observed |
Allergies | Allergic Asthma |
Allergic Rhinitis | |
Allergies in General | |
Allergy to Nuts | |
Allergy to Pets | |
Allergy to Shrimp | |
Allergy to mites | |
Allergy to pollen | |
Asthma | |
Atopic Dermatitis | |
Cockroach allergy | |
Cold-induced hives | |
Contact dermatitis | |
Eczema | |
Egg White Allergy | |
Grass allergy | |
Histamine Intolerance | |
IgE | |
Mast Cell Activation Syndrome (MCAS) | |
Milk Allergy | |
Peach Allergy | |
Peanut Allergy | |
Cancer | Thyroid Neoplasm |
Cardiovascular | Prothrombin (G20210A Mutation) |
Cardiovascular and Cerebrovascular | Phospholipase Cg2 Defect |
Cells | Autophagy |
Diabetes | Early Type 2 Diabetes |
MODY Type 1 Diabetes | |
MODY Type 2 Diabetes | |
MODY Type 3 Diabetes | |
MODY Type 4 Diabetes | |
MODY Type 5 Diabetes | |
MODY Type 6 Diabetes | |
MODY Type Diabetes | |
Type 1 Diabetes | |
Type 2 diabetes | |
Digestive system | Hirschsprung's Disease (HD) |
Permeable Intestine Syndrome | |
Primary Biliary Cirrhosis (CBP) | |
Ulcerative Colitis | |
Endocrine system | Autoimmune Thyroid Disease |
Hashimoto's Thyroiditis | |
Hashimoto's Thyroiditis (in children) | |
Hyperparathyroidism | |
Hyperthyroidism | |
Hypothyroidism | |
Hypothyroidism (Goiter) | |
T3 | |
Thyroid Orbitopathy (OT) | |
Thyroid dyshormonogenesis | |
Thyrotoxicosis | |
Genetic diseases | Familial Amyloidotic Polyneuropathy (FAP) |
Family Mediterranean Fever | |
Hereditary angioedema | |
Hyperimmunoglobulin E (Hyper IgE) Syndrome | |
Rasopathies | |
Selective IgA Deficiency | |
Hematologic system | Activated partial thromboplastin time (aPTT) |
Alpha-Defensins Levels | |
Hemolytic Anemia | |
High ferritin (in men) | |
Post-Transfusion Purpura (PPT) | |
Tendency to have Increased Eosinophils in Contact with Allergens | |
Thrombophilia (Factor V - Protein C) | |
Hormone | Change of Timo |
Reduction of Thyroid Hormonal Metabolism | |
TSH | |
Thyroid Function | |
Thyroid Hormone Metabolism (T3: T4 Reduced Ratio) | |
Immune system | Acquired Immune Response |
Ankylosing spondylitis | |
Anti-Beta-2-Glycoprotein Antibody | |
Anti-DNA Antibody | |
Anticardiolipin Antib. | |
Antiphospholipid Antibody Syndrome | |
Antithrombin Deficiency | |
Autoimmune Lymphoproliferative Syndrome (ALPS) | |
B Lymphocyte Deficiency | |
C3 (immune) deficiency | |
Chronic Granulomatous Disease (CGD) | |
Combined immunodeficiency due to magnesium deficiency (XMEN) | |
Common Variable Immunodeficiency - type 1 | |
Common Variable Immunodeficiency - type 2 | |
Common Variable Immunodeficiency - type 8 | |
Crohn's disease | |
Defect in Thyroid Hormonogenesis | |
Dermatomyositis | |
Factor V Leiden Mutation | |
Familial hemophagocytic lymphohistiocytosis (HLH) | |
Graves' Disease | |
Guillain-Barré Syndrome | |
HLA-DQ2.2 | |
HLA-DQ2.5 | |
HLA-DQ4 | |
HLA-DQ7 | |
HLA-DQ8 | |
Herpes | |
Immunodeficiency with Hyper IgM - type 1 | |
Increased Susceptibility to Contracting HIV-1 | |
Lichen Planus | |
Lupus | |
Lupus anticoagulant | |
Lymphedema | |
MYD88 deficiency | |
Mannose Binding Protein Deficiency | |
Mutation of the SERPINE1 Gene (PAI-1) | |
Myeloperoxidase Deficiency | |
Neurosarcoidosis | |
Polyglandular deficiency syndromes | |
Primary Sclerosing Cholangitis | |
Prolactin Promoter Polymorphism | |
Protein C Deficiency | |
Protein S Deficiency | |
Psoriasis | |
Psoriatic arthritis | |
Risk of Decreased Metabolism of Thyroid Hormones | |
Severe Combined Immunodeficiency Syndrome | |
Severe Combined Immunodeficiency with Sensitivity to Ionizing Radiation | |
Severe Congenital Neutropenia | |
Severe Congenital Neutropenia and Cyclic Neutropenia | |
T Lymphocyte Deficiency | |
Type 2 X-linked Lymphoproliferative Syndrome | |
Wegener's granulomatosis | |
X-Linkerd Lymphoproliferative (XLP) Syndrome | |
X-linked Lymphoproliferative Syndrome (XLP) | |
Inflammations | Behçet's Disease |
Frontal Fibrosing Alopecia | |
Idiopathic inflammatory myopathy | |
Inflammatory Bowel Disease (IBD) | |
Polymyositis | |
Presence of the HLA-B27 Allele | |
Sarcoidosis | |
Scleroderma | |
Sjogren's Syndrome | |
Metabolic | Celiac disease |
Gluten Intolerance | |
Glycation | |
Greater Insulin Sensitivity with Physical Exercise | |
Lactose intolerance | |
Metabolic disorders | Fetuin-A |
Methylation | MTHFR 1298 mutation (rs1801131) |
MTHFR 677 mutation (rs1801133) | |
Muscular system | Myasthenia Grave |
Neurodegenerative diseases | Charcot-Marie Disease |
Louis-Bar Syndrome (Ataxia Telangiectasia) | |
Multiple sclerosis | |
Systemic Sclerosis | |
Respiratory system | Chronic obstructive pulmonary disease |
Skeletal system (bones) | Arthritis |
Carpal tunnel syndrome | |
Osteoarthritis | |
Osteoporosis | |
Rheumatoid arthritis | |
Risk of amputation in case of diabetic foot ulcer | |
Skin | Alopecia Areata |
Generalized Vitiligo | |
Rosacea | |
Vitiligo | |
Urinary system | Membranoproliferative Glomerulonephritis (GNMP) |
Nephrotic syndrome | |
Vision (Ophthalmology) | Diabetic retinopathy |
Categories | Conditions Observed |
Cancer | Acute Lymphoblastic Leukemia (ALL) |
Childhood Acute Lymphoblastic Leukemia | |
Childhood Leukemia | |
Erythrocytosis | |
JAK2 V617F mutation | |
Myelodysplastic Syndrome | |
Myeloproliferative Disorder | |
Peripheral T cell lymphoma | |
Polycythemia Vera | |
Cardiovascular | Arginine-succinic aciduria |
Atherosclerosis (hyperlipidemia) | |
Benefit of Niacin in Reducing Lipoprotein (a) | |
Cardiovascular Disease (Cholesterol Level) | |
Dysfunctional HDL | |
Familial Hyperlipoproteinemia Type III | |
Hereditary familial hypercholesterolemia | |
Hypercholesterolemia (Type B) | |
Jervell and Lange-Nielsen Syndrome | |
Narrowing of Blood Vessels (Stenosis) | |
Platelets (Highest Count) | |
Platelets (Lowest Count) | |
Prothrombin (G20210A Mutation) | |
Pulmonary Embolism | |
Venous Thromboembolism (VTE) | |
Cardiovascular and Cerebrovascular | Homocysteine Accumulation |
Lipoprotein (a) | |
Clopidogrel | Response to Clopidogrel |
Diabetes | Fasting Glucose Level Increase |
Digestive system | Gilbert's Syndrome |
General | ALT / AST Index |
Genetic diseases | A1 A2 Alloantigen Polymorphism |
Alpha Antitrypsin Deficiency (AAT) | |
Alpha-2-Macroglobulin Polymorphism | |
Cholesterol Ester Transfer Protein Deficiency | |
Elliptocytosis | |
Factor II Deficiency (Prothrombin) | |
Factor VII Protease Polymorphism (Marburg) | |
Gamma-Glutamylcysteine Synthetase Deficiency | |
Glutathione Synthetase Deficiency | |
Hereditary angioedema | |
Hyperimmunoglobulin E (Hyper IgE) Syndrome | |
Leukocyte Adhesion Deficiency - Type 1 | |
Mevalonate Kinase Deficiency | |
Multiple Sulphatase Deficiency (Austin's Disease) | |
OKT4 deficiency | |
Upshaw Schulman Syndrome | |
Von Willebrand Disease | |
Wiskott-Aldrich Syndrome | |
Hematologic system | Activated partial thromboplastin time (aPTT) |
Afibrinogenemia | |
Albumin | |
Alpha-Defensins Levels | |
Argininemia | |
Aspartate Aminotransferase (AST) | |
Atypical Hemolytic Uremic Syndrome (aHUS) | |
Benefit of Physical Exercise for HDL | |
Beta Thalassemia | |
Bilirubin | |
Bleeding Disorder (Platelets) | |
Blood Glucose Level | |
Carbamoyl Phosphate Synthetase I Deficiency | |
Circulating Glycated Hemoglobin (HbA1c) | |
Congenital Dyserythropoietic Anemia | |
Congenital Thrombotic Thrombocytopenic Purpura | |
Congenital afibrinogenemia | |
Crigler-Najjar Syndrome | |
D-dimers (Fibrin Degradation Products) | |
Deficiency of Vitamin K-Dependent Coagulation Factors | |
Essential Thrombocythemia | |
Excess Calcium in Blood | |
Factor V deficiency | |
Factor VII Deficiency | |
Factor XII Polymorphism | |
Factor XIII deficiency | |
Fanconi's anemia | |
G6PD deficiency | |
Galactose Epimerase Deficiency | |
Glanzmann's thrombasthenia | |
HDL (Cholesterol) | |
HDL Deficiency (Family) | |
Haptoglobin | |
Hemochromatosis | |
Hemolytic Anemia | |
Hemophilia - Factor VIII Deficiency | |
Hemophilia A | |
Hemophilia B | |
Hereditary Persistence of Fetal Hemoglobin (HPFH) | |
Hereditary Stomatocytosis | |
High Ferritin | |
High ferritin (in men) | |
Higher HDL on Low Carbohydrate Diets | |
Hyperbilirubinemia | |
Hyperhomocysteinemia | |
Hypoproteinemia | |
Idiopathic Hypereosinophilic Syndrome | |
Intermediate Beta Thalassemia | |
L-ferritin deficiency | |
LDL (Cholesterol) | |
Low Ferritin in Men | |
Low Ferritin in Women | |
Low ferritin in children under 2 years | |
Lower Hemoglobin Levels | |
Microcytic Anemia | |
Neuroferritinopathy | |
Ornithine Transcarbamylase Deficiency | |
Oxidized LDL | |
Paroxysmal Nocturnal Hemoglobinuria (PNH) | |
Platelet Count | |
Post-Transfusion Purpura (PPT) | |
Reduction in Factor VIII Activity (Coagulation) | |
Reduction in Factor XII Activity (Coagulation) | |
Shwachman-Diamond Syndrome | |
Sickle cell anemia | |
Spherocytosis | |
TIBC | |
Tendency to have Increased Eosinophils in Contact with Allergens | |
Thiamine-Responsive Megaloblastic Anemia | |
Thrombocytopenia | |
Thrombophilia (Factor V - Protein C) | |
Thrombophilia (Factor VII) | |
Transferrin | |
Triglycerides | |
Villejuif Hemoglobin | |
X Factor Deficiency | |
Hereditary diseases | Hereditary Sideroblastic Anemia |
Hormones | Hepcidin |
Immune system | Anti-Beta-2-Glycoprotein Antibody |
Anti-DNA Antibody | |
Anticardiolipin Antib. | |
Antiphospholipid Antibody Syndrome | |
Antithrombin Deficiency | |
Autoimmune Lymphoproliferative Syndrome (ALPS) | |
Congenital Erythropoietic Porphyria (Gunther's Disease) | |
Factor V Leiden Mutation | |
Familial hemophagocytic lymphohistiocytosis (HLH) | |
Human Leukocyte Antigen (HLA) | |
Lupus | |
Lupus anticoagulant | |
Malaria Resistance | |
Mannose Binding Protein Deficiency | |
Mutation of the SERPINE1 Gene (PAI-1) | |
Phenylketonuria | |
Primary Functional Neutrophil Disorder | |
Prolactin Promoter Polymorphism | |
Protein C Deficiency | |
Protein S Deficiency | |
Resistance to HIV (AIDS) | |
Resistance to Norovirus (NoV) | |
Type 2 X-linked Lymphoproliferative Syndrome | |
Wegener's granulomatosis | |
X-linked Lymphoproliferative Syndrome (XLP) | |
Metabolic | Ceruloplasmin |
Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency | |
Greater Insulin Sensitivity with Physical Exercise | |
Lactate dehydrogenase (LDH) | |
Methionine Adenosyltransferase Deficiency | |
Metabolic disorders | Cobalamin Intracellular Metabolism Disease |
Dyslipidemia | |
Galactosemia | |
Homocystinuria | |
Hyperferritinemia | |
Low Ferritin | |
Myoadenylate Deaminase Deficiency | |
Methylation | MTHFR rs1801131 |
MTHFR 1298 mutation (rs1801131) | |
MTHFR 677 mutation (rs1801133) | |
MTHFR rs1801133 | |
Need for Nutrients | Betaine |
Iron | |
Personal characteristics | Toxic Sensitivity to Benzene |
Pharmacogenetics | Warfarin |
Respiratory system | Aspergillosis |
Oxygen Volume (O2) Max (VO2 Max) | |
Skin | Basal Blade Disease |
Erythropoietic Protoporphyria | |
Hyperchromias | |
Urinary system | Gout |
Hematuria | |
Uric Acid (Concentration) | |
Vitamins | Vitamin B3 (Niacin) |
Categories | Conditions Observed |
Auditory system | Non-syndromic deafness |
Sudden Deafness Syndrome | |
Usher Syndrome | |
Breast cancer | Breast Neoplasm (Family) |
Cancer | BAP1 - Tumor Predisposition Syndrome |
Colorectal Neoplasm (Family) | |
Cowden's Syndrome | |
Hereditary Cancer Predisposition Syndrome | |
Hereditary Tyrosinemia Type 1 | |
Li-Fraumeni Syndrome | |
Lynch Syndrome | |
Retinoblastoma | |
Tumor predisposition syndrome (BAP1) | |
Cardiovascular | Brugada Syndrome |
Familial Hyperlipoproteinemia Type III | |
Familial Hypertrophic Cardiomyopathy | |
Jervell and Lange-Nielsen Syndrome | |
Progressive Familial Heart Block | |
Romano-Ward Syndrome | |
Sinus Nodule Syndrome | |
Diabetes | MODY Type 3 Diabetes |
MODY Type 4 Diabetes | |
MODY Type 5 Diabetes | |
MODY Type 6 Diabetes | |
MODY Type Diabetes | |
Digestive system | Alagille Syndrome (Arteriohepatic Dysplasia) |
Congenital Lactase Deficiency | |
Congenital diarrhea | |
Cystic fibrosis | |
Dubin-Johnson Syndrome | |
Familial Intrahepatic Cholestasis | |
Family diarrhea | |
Irritable Bowel Syndrome | |
Juvenile Polyposis Syndrome | |
Trichohepatoenteric Syndrome (THE) | |
Type 1 Progressive Intrahepatic Cholestasis | |
Type 2 Progressive Intrahepatic Cholestasis | |
Type 3 Progressive Intrahepatic Cholestasis | |
Type 4 Progressive Intrahepatic Cholestasis | |
General | Williams Syndrome |
Genetic diseases | Achondroplasia |
Adrenoleukodystrophy | |
Alpha Antitrypsin Deficiency (AAT) | |
Alpha-1 Antitrypsin Deficiency | |
Alport's Syndrome | |
Angelman Syndrome | |
Axenfeld Rieger Syndrome | |
Bardet-Biedl Syndrome | |
Berardinelli-Seip Syndrome | |
Blau's Syndrome | |
Blepharophimosis Syndrome | |
Bloom Syndrome | |
Branched Chain Amino Acid Dehydrogenase Kinase Deficiency | |
Cardio-facio-cutaneous syndrome | |
Carpenter's Syndrome | |
Cat's Eye Syndrome | |
Char syndrome | |
Cockayne's Syndrome | |
Cohen's Syndrome | |
Costello Syndrome | |
Doors Syndrome | |
Down's syndrome | |
Ellis Van Creveld Syndrome | |
Epilepsy Responsive to pyridoxine | |
Fabry disease | |
Familial Adenomatous Polyposis | |
Familial Amyloidotic Polyneuropathy (FAP) | |
Familial Dysautonomy (Riley-Day Syndrome) | |
Familial Glucocorticoid Deficiency (DFG) | |
Familial cold autoinflammatory syndrome (FCAS) | |
Familial hypobetalipoproteinemia | |
Family Mediterranean Fever | |
Family Periodic Fever | |
HNRNPH2 | |
Hereditary Breast and Ovary Cancer Syndrome | |
Hereditary angioedema | |
Hermansky-Pudlak Syndrome - 1 | |
Hermansky-Pudlak Syndrome - 4 | |
Hermansky-Pudlak Syndrome - 6 | |
Hurler's Syndrome | |
Hypereplexy | |
Hyperimmunoglobulin E (Hyper IgE) Syndrome | |
Hyperornithinemia-Hyperammonemia-Homocitrulinuria Syndrome | |
Hypohydrotic Ectodermal Dysplasia | |
Joubert Syndrome | |
Kabuki Syndrome | |
Kindler Syndrome | |
Ligase 4 Deficiency Syndrome (LIG4) | |
Lucey-Driscoll Syndrome | |
Maple Syrup Urine Disease (Leucinosis) | |
Marfan syndrome | |
Metachromatic leukodystrophy | |
Miller-Dieker Syndrome | |
Morquio Syndrome | |
Mucolipidosis Type 4 (Gangliosidosis) | |
Mucopolysaccharidosis | |
Mucopolysaccharidosis Type II | |
Mucopolysaccharidosis Type IIIB | |
Mucopolysaccharidosis Type IVA | |
Multiple Sulphatase Deficiency (Austin's Disease) | |
Noonan's Syndrome | |
PANDAS Syndrome | |
PTEN Tumor Hamartoma Syndrome | |
Pfeiffer's Syndrome | |
Phelan-McDermid Syndrome | |
Pigment Incontinence Syndrome | |
Pontocerebellar Hypoplasia | |
Prader-Willi Syndrome | |
Primary Hyperoxaluria | |
Proteus Syndrome | |
Pseudo Arisulfatase A Deficiency | |
Rasopathies | |
Rett Syndrome | |
Salla's disease | |
Schaaf-Yang Syndrome | |
Schwartz Jampel Syndrome Type 1 | |
Seckel's Syndrome | |
Selective IgA Deficiency | |
Smith-Lemli-Opitz Syndrome | |
Smith-Magenis Syndrome | |
Sotos Syndrome | |
Townes Syndrome | |
Transthyretin-mediated Hereditary Amyloidosis (TTR) | |
Treacher-Collins Syndrome | |
Tuberous Sclerosis | |
Type 0B Glycogenosis | |
Type 1 Gaucher Disease | |
Ubiquitins | |
Upshaw Schulman Syndrome | |
Van der Woude Syndrome | |
Walker-Warburg Syndrome | |
Weaver syndrome | |
Weill-Marchesani Syndrome | |
Werner's Syndrome | |
Wilson's Disease | |
Wiskott-Aldrich Syndrome | |
Wolfram syndrome | |
Zellweger Syndrome | |
Hematologic system | Afibrinogenemia |
Atypical Hemolytic Uremic Syndrome (aHUS) | |
Beta Thalassemia | |
Congenital Dyserythropoietic Anemia | |
Fanconi's anemia | |
HDL Deficiency (Family) | |
Hemochromatosis | |
Hemophilia - Factor VIII Deficiency | |
Hemophilia A | |
Hereditary Stomatocytosis | |
Intermediate Beta Thalassemia | |
Sickle cell anemia | |
Spherocytosis | |
Thrombophilia (Factor V - Protein C) | |
X-linked agammaglobulinemia | |
Hereditary diseases | Fragile X Syndrome |
Friedreich's Ataxia | |
Pompe disease | |
Hormones | 5α-Reductase |
Aromatase Deficiency | |
Immune system | Autoimmune Lymphoproliferative Syndrome (ALPS) |
Congenital Erythropoietic Porphyria (Gunther's Disease) | |
Familial hemophagocytic lymphohistiocytosis (HLH) | |
Neurofibromatosis | |
Severe Combined Immunodeficiency Syndrome | |
Type 2 X-linked Lymphoproliferative Syndrome | |
X-linked Lymphoproliferative Syndrome (XLP) | |
Inflammations | Sjogren's Syndrome |
Yao's Syndrome | |
Metabolic | Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency |
Mitochondrial Complex Deficiency 1 | |
Metabolic disorders | Acute Intermittent Porphyria |
Adenosine Monophosphate Deaminase Deficiency | |
Cerebrotendinous Xanthomatosis (CTX) | |
Fructosemia | |
Homocystinuria | |
Methylmalonic Acidemia | |
Myoadenylate Deaminase Deficiency | |
Sanfilippo Syndrome | |
Variegate Porphyria | |
Muscular system | Becker Muscular Dystrophy |
Duchenne Muscular Dystrophy | |
Emery-Dreifuss Muscular Dystrophy | |
Hypotonia in Down Syndrome | |
Leigh's Syndrome | |
Malignant Hyperthermia | |
Melas Syndrome | |
Muscular Dystrophy - Congenital Dystroglycanopathy | |
Myasthenia Grave | |
Neurodegenerative diseases | Canavan disease |
Charcot-Marie Disease | |
Congenital Central Hypoventilation | |
Huntington's Disease | |
Louis-Bar Syndrome (Ataxia Telangiectasia) | |
Pick's Disease | |
Spinocerebellar Ataxia | |
Tay-Sachs disease | |
Torsional dystonia | |
Wolfram Syndrome-1 | |
Neurological | GLUT1 Deficiency Syndrome |
West syndrome | |
Personal characteristics | Antley-Bixley Syndrome with Genital Anomaly |
Psychiatric | Restless Legs Syndrome (Willis-Ekbom disease) |
Tourette's Syndrome | |
Reproductive system | Perrault Syndrome |
Polycystic Ovary Syndrome | |
Skeletal system (bones) | Hypochondroplasia |
Léri-Weill dyschondrosteosis | |
Skin | Ehlers Danlos Syndrome (collagen) |
Erythropoietic Protoporphyria | |
Family candidiasis | |
KID Syndrome | |
Urinary system | Bartter's Syndrome |
Familial Amyloid Nephropathy with Urticaria and Deafness | |
Polycystic Kidney Disease (DRP) | |
Renal agenesis | |
Vision (Ophthalmology) | Choroideremia |
Dry Eye Syndrome | |
Knobloch Syndrome | |
Stickler Syndrome | |
Vitamins need | Biotinidase Deficiency |
Categories | Conditions Observed |
Allergies | Alcohol Aversion |
Gluten Sensitivity | |
Amino acids | Glutamate Production |
L-theanine | |
L-tyrosine | |
Serine Deficiency | |
Antioxidants / Supplements | Coenzyme Q10 |
Glutathione | |
Need for a diet rich in antioxidants | |
Probiotics | |
Behavioral Changes | Mood Disorder |
Behaviors | Dopamine Levels |
Benefit | Chamomile |
S-adenosylmethionine (SAMe) | |
Stevia Sweetener Benefit | |
Cancer | Multiple Endocrine Neoplasm |
Thyroid Neoplasm | |
Cardiovascular | Arginine-succinic aciduria |
Familial Hyperlipoproteinemia Type III | |
Hereditary familial hypercholesterolemia | |
Hypercholesterolemia (Type B) | |
Cardiovascular and Cerebrovascular | Homocysteine Accumulation |
Hypertension | |
Phospholipase Cg2 Defect | |
Sensitivity to Salt (Hypertension) | |
Diabetes | CAPN10 |
DPP-4 | |
Diabetic Neuropathy | |
ENPP1 | |
Early Type 2 Diabetes | |
Fasting Glucose Level Increase | |
Fasting Insulin | |
GLP-1 | |
GLUT4 | |
Glucose Intolerance | |
IRS-1 | |
Insulin Sensitivity | |
Insulinogenic Index | |
Lower Insulin Secretion | |
MODY Type 1 Diabetes | |
MODY Type 2 Diabetes | |
MODY Type 3 Diabetes | |
MODY Type 4 Diabetes | |
MODY Type 5 Diabetes | |
MODY Type 6 Diabetes | |
MODY Type Diabetes | |
PI3K | |
Reduction in Insulin Secretion | |
Regulation of Oxidative Phosphorylation in Skeletal Muscle | |
Type 1 Diabetes | |
Type 2 diabetes | |
Weight Reduction in Liraglutide Treatment | |
Β Cell Function Impairment | |
Digestive system | Family diarrhea |
Hyperglycinuria | |
Hyperlipoproteinemia | |
Peroxisomal Enzyme Deficiency | |
Drug Reactions | Better Response to Methotrexate |
Endocrine system | Addison's Disease |
Autoimmune Thyroid Disease | |
Benefit of adopting a low glycemic index diet | |
Congenital Adrenal Hypoplasia (CAC) | |
Hashimoto's Thyroiditis | |
Hyperparathyroidism | |
Hyperthyroidism | |
Hypophosphatemic Rickets | |
Hypothyroidism | |
Hypothyroidism (Goiter) | |
Monogenic Diabetes | |
Resistance to Thyroid Hormone | |
Severe Neonatal Hyperparathyroidism | |
T3 | |
Thyroid Orbitopathy (OT) | |
Thyroid dyshormonogenesis | |
Thyrotoxicosis | |
Transient Neonatal Diabetes | |
Essential Amino Acids | L-lysine |
L-methionine | |
Fatty acids | Omega 6 |
Omega 9 | |
General | Alcohol Intolerance |
Aversion to Vegetables and Coffee | |
GS | |
INSR | |
p70S6K | |
Genetic diseases | Alpha Antitrypsin Deficiency (AAT) |
Alpha Hydroxyphenylpyruvate Hydroxylase Deficiency | |
Chitotrioidase Deficiency | |
Cholesterol Ester Transfer Protein Deficiency | |
Congenital Adrenal Hyperplasia (CAC) | |
Cytichrome-C Oxidase Deficiency | |
Deficiency of Tetrahydrobiopterin Synthesis | |
Dihydropyridine Dehydrogenase Deficiency | |
Familial Adenomatous Polyposis | |
Familial Glucocorticoid Deficiency (DFG) | |
Gamma-Glutamylcysteine Synthetase Deficiency | |
Glutathione S-transferase-1 Mutation | |
Glutathione Synthetase Deficiency | |
Lysosomal Acid Lipase Deficiency | |
Mevalonate Kinase Deficiency | |
Mutation of Glutathione Peroxidase-1 | |
Mutation of Glutathione S-transferase (GST) theta 1 | |
Mutation of Glutathione S-transferase M1 | |
Mutation of Iodothyronine Deiodinase 2 | |
Mutation of Superoxide Dismutase-1 | |
Mutation of Superoxide Dismutase-2 | |
Mutation of Superoxide Dismutase-3 | |
OKT4 deficiency | |
Platelet Glycoprotein Deficiency IV | |
Pyridoxine Deficiency | |
Rasopathies | |
Werner's Syndrome | |
Hematologic system | Albumin |
Anemia | |
Aplastic anemia | |
Apolipoprotein E | |
Fanconi's anemia | |
G6PD deficiency | |
HDL (Cholesterol) | |
HDL Deficiency (Family) | |
Hemolytic Anemia | |
High Ferritin | |
High ferritin (in men) | |
Hyperhomocysteinemia | |
Hyperinsulinemia | |
Hypoproteinemia | |
L-ferritin deficiency | |
Sickle cell anemia | |
Triglycerides | |
Hereditary diseases | Lipotransferase 1 deficiency |
Hormone | Acromegaly |
Adiponectin Flag | |
Androstenedione | |
Anti-Müllerian hormone (AMH) | |
Change of Timo | |
Cushing's Syndrome | |
Folic Acid Metabolism | |
Growth Hormone (GH) Deficiency | |
Leptin | |
Luteinizing Hormone (LH) | |
Reduction of Thyroid Hormonal Metabolism | |
Renina's Greatest Activity | |
Resistin | |
SHBG levels | |
TSH | |
Thyroid Function | |
Thyroid Hormone Metabolism (T3: T4 Reduced Ratio) | |
Hormones | 5α-Reductase |
Adiponectin Levels | |
Adrenal function | |
Adrenaline | |
Adrenocorticotrophic Hormone | |
Aromatase Deficiency | |
Benefit of Melatonin | |
Cortisol Level | |
DHEA/DHEAS | |
Estradiol | |
Estriol | |
Estrone | |
Excess of Aromatase | |
Growth Hormone Response | |
Impact of GH Replacement Treatment on Lipid Profile | |
Increased Cortisol (in women) | |
Inhibin | |
Insulin Resistance | |
Noradrenaline | |
Parathyroid Hormone (PTH) | |
Progesterone | |
Somatostatin | |
T4 | |
Testosterone | |
Vasopressin (Antidiuretic Hormone - ADH) | |
Immune system | Autoimmune Disease |
C3 (immune) deficiency | |
Crohn's disease | |
Defect in Thyroid Hormonogenesis | |
Human Leukocyte Antigen (HLA) | |
Mannose Binding Protein Deficiency | |
Inflammations | Increased IL-6 with Vitamin E (Alpha-tocopherol) intake |
Sjogren's Syndrome | |
Metabolic | Ability to Digest Starch |
Ability to digest starch | |
Ammonia and Glutamate Production | |
BCKDK gene | |
CBS Gene - Transsulfuration | |
Caffeine Metabolization | |
Carbohydrate Metabolism | |
Decline of NAD | |
Detox (Detoxification) | |
Detoxification | |
Glutamate to GABA Conversion | |
Gluten Intolerance | |
Glycation | |
Greater Insulin Sensitivity with Physical Exercise | |
HDL increase with Omega 6 intake | |
Improving Insulin Sensitivity with Physical Exercise | |
Lactate dehydrogenase (LDH) | |
Leptin receptor polymorphism | |
Lipid Metabolism | |
Metabolic syndrome | |
Methionine Adenosyltransferase Deficiency | |
Methylation | |
Micronutrient Metabolism | |
Obesity | |
Protein Metabolization | |
Resting Metabolism | |
Starch Metabolism | |
Trend of Eating Sweets | |
Trend of Overeating (Gluttony) | |
Trend to regain weight | |
Weight Gain Trend | |
Metabolic disorders | 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency |
3-Hydroxy-3-Methylglutaryl-CoA Synthetase 2 Deficiency | |
3-Hydroxyacyl-CoA Dehydrogenase Deficiency | |
Abetalipoproteinemia (Bassen-Kornzweig Syndrome) | |
Abetalipoproteinemia (Diet) | |
Adenosine Monophosphate Deaminase Deficiency | |
Alpha Methyl Acetoacetic Aciduria | |
Bile Acid Synthesis Deficiency | |
Brain Folate Transport Deficiency | |
Carnitine Acylcarnitine Translocase Deficiency | |
Carnitine Palmitoyltransferase I Deficiency | |
Carnitine Palmitoyltransferase II Deficiency | |
Cerebral Creatine Deficiency Syndrome | |
Cerebrotendinous Xanthomatosis | |
Congenital Sucrase Isomaltase Deficiency | |
Dopa-Responsive Dystonia (DRDSPRD) | |
Dyslipidemia | |
Enteropathic Acrodermatitis | |
Familial hypercholanemia | |
Fetuin-A | |
Fructose-1,6 Bisphosphatase Deficiency | |
Fructosemia | |
Galactokinase Deficiency | |
Galactosemia | |
Glucose/Galactose Malabsorption | |
Glutaric Aciduria | |
Glycogen Storage Disease | |
Glycogen Storage Disease Type IXa | |
Glycogen Storage Disease type IXb | |
Glycogenosis Type 0A | |
Glycogenosis Type IB/IC | |
Hereditary Folate Malabsorption | |
Hereditary Fructose Intolerance | |
Hyperferritinemia | |
Hyperphenylalaninemia due to BH4 Deficiency | |
Hyperprolinemia | |
Hypophosphatasia | |
It-type Congenital Glycosylation Disorder | |
Lysinuric Protein Intolerance | |
Lysosomal Acid Lipase Deficiency | |
Maple Syrup Disease (Leucinosis) | |
Medium Chain Acyl-CoA Dehydrogenase Deficiency | |
Methylmalonic Acidemia | |
Methylmalonic Aciduria and Homocystinuria | |
Methylmalonic aciduria | |
Mild Hyperphenylalaninemia without BH4 Deficiency | |
Monocarboxylate Carrier 1 Deficiency | |
Multiple Acyl-CoA Dehydrogenase Deficiency | |
N-Acetylglutamate Synthetase Deficiency | |
Niacin's Benefit in Reducing Liver Fat | |
Phosphoserine Aminotransferase Deficiency | |
Pituitary Deficiency (Hypopituitarism) | |
Primary Systemic Carnitine Deficiency | |
Propionic Acidemia | |
Purine Nucleoside Phosphorylase Deficiency | |
Segawa Syndrome | |
Succinyl-CoA 3-oxoacid-CoA transferase deficiency | |
Thiamine 2 Metabolism Dysfunction Syndrome | |
Thiamine 4 Metabolism Dysfunction Syndrome | |
Thiamine 5 Metabolism Dysfunction Syndrome | |
Trifunctional Mitochondrial Protein Deficiency | |
Type IA glycogenosis | |
Type III glycogenosis | |
Type IV glycogenosis | |
Type Ib Congenital Glycosylation Disorder | |
Type Iz Congenital Glycosylation Disorder | |
Type VI glycogenosis | |
Tyrosine Hydroxylase Deficiency | |
Tyrosinemia | |
Very Long Chain Acyl-Coa Dehydrogenase Deficiency | |
Vitamin E Deficiency | |
Xenobiotic Metabolism (Including Caffeine and P-450) | |
Mitochondria | Oxidative Phosphorylation |
Need for Nutrients | Apigenin need |
Benefit of Bergamot | |
Betaine | |
Bromelain | |
Calcium | |
Choline | |
Chrome | |
Copper | |
Hop | |
Iodine | |
Iron | |
Lutein | |
Lycopene | |
Magnesium | |
Manganese | |
Phosphatidylcholine Levels | |
Phosphorus | |
Potassium | |
Quercetin | |
Reaction to Glutamate | |
Selenium | |
Tetrahydrobiopterin | |
Vitexin need | |
Zeaxanthin | |
Zinc | |
Neurodegenerative diseases | Peripheral neuropathy |
Oxidation | Antioxidant Capacity |
Glutamic Acid Metabolism | |
Individuals not expressing CYP3A5 | |
Oxidative stress | |
Personal characteristics | Alcohol Metabolism |
Greater Stimulus with Caffeine | |
Hypersensitivity to Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) | |
Increased Probability of Fatigue | |
Mitochondrial Energy Production | |
Pineal Hyperplasia | |
Spondyloepiphyseal Dysplasia | |
Psychiatric | Anorexia Nervosa |
Reactions to Treatments | Levothyroxine Combination therapy with Liothyronine |
Reproductive system | Age at Menarche |
Gestational diabetes | |
Polycystic Ovary Syndrome | |
Skeletal system (bones) | Development Defects |
Risk of amputation in case of diabetic foot ulcer | |
Skin | Elastin Deficiency |
Urinary system | Uric Acid (Concentration) |
Vision (Ophthalmology) | Diabetic retinopathy |
Vitamins | Folate |
Vitamin A | |
Vitamin B12 | |
Vitamin B2 | |
Vitamin B6 | |
Vitamin B7 (Biotin) | |
Vitamin B9 (Folic Acid) | |
Vitamin C | |
Vitamin D | |
Vitamin E | |
Vitamin K | |
Vitamins need | Reduced Conversion of Beta Carotene to Retinol |
Riboflavin Deficiency | |
Weight | Absorption of Fats |
Benefit of Physical Exercise for Weight Loss | |
Fat Metabolism | |
Fibers and slimming | |
Ghrelin | |
Greater Resistance to Weight Loss on Low Calorie Diets | |
High Levels of Fatty Acids after Fat Ingestion | |
Increased waist measurement with the habit of smoking a lot | |
Intake of saturated fat and increased body fat | |
Irisina | |
Lower Use of Glucose after Carbohydrate Ingestion | |
Lower Weight Gain on High Fat Diets | |
Obesity (monogenic) | |
Obesity in Adolescents | |
Preference for bitter foods | |
Preference for fatty foods | |
Preference for sweet foods | |
Quantitative Body Mass Index (BMI) | |
Reduction of body fat with intervention of polyphenols | |
Slimming with Restricted Carbohydrates Intake | |
Slimness | |
Trend of Higher Protein Consumption | |
Trend of Monounsaturated Fat Intake and Weight Gain | |
Trend of Polyunsaturated Fat Intake and Weight Gain | |
Trend towards Higher Carbohydrate Consumption | |
Visceral Fat Accumulation | |
Waist Measure | |
Waist Measurement (in Women) | |
Weight Loss on Fat Reduction Diets | |
Weight Loss with the Consumption of Complex Carbohydrates | |
Weight Management | |
Weight gain with exercise | |
Weight loss and abdominal fat loss in caloric restriction | |
Weight loss with more protein than carbohydrate intake |
Categories | Conditions Observed |
Amino acids | N-acetylcysteine |
Cardiovascular | Long QT Syndrome |
Romano-Ward Syndrome | |
Venous Thromboembolism (VTE) | |
Coronavirus (COVID-19) | COVID-19-induced respiratory failure |
Coronavirus 2019 (COVID-19) | |
Covid-19 protection | |
Cytokine Storm | |
Increased Risk of Intensive Care with Covid-19 | |
Risk of severe COVID-19 | |
Cytokine Storm | CCL2 (MCP-1) |
CXCL10 | |
CXCR2 | |
IL-1 | |
IL-10 | |
IL-10RB | |
IL-17 | |
IL-1B | |
IL-6 | |
IL-8 (CXCL8) | |
MCP1 | |
MEFV | |
TGF-B | |
TNFRSF1B | |
VEGF | |
Genes | IFN-A |
IL-1R | |
IL-8 | |
Hematologic system | Alpha-Defensins Levels |
Thrombocytopenia | |
Immune system | CCL-3 |
CCL-5 | |
IFN-γ (Interferon-Gamma) | |
IFNAR1 | |
IFNAR2 | |
IL-12RB1 | |
Need for Nutrients | Lycopene |
Magnesium | |
Quercetin | |
Selenium | |
Zinc | |
Respiratory system | Avian Influenza (H7N9) |
Flu (Influenza) | |
H1N1 flu | |
H3N2 - Variant of Influenza A | |
Influenza B | |
Pneumonia from H1N1 | |
Poor Prognoses in Respiratory Disease | |
Pulmonary Sepsis | |
Pulmonary fibrosis | |
Respiratory Syncytial Virus (RSV) | |
SARS Pneumonia | |
Severe Acute Respiratory Syndrome | |
Tuberculosis | |
Vitamins | Vitamin A |
Vitamin B1 (Thiamine) | |
Vitamin B12 | |
Vitamin B6 | |
Vitamin B9 (Folic Acid) | |
Vitamin C | |
Vitamin D | |
Vitamin E |
Categories | Conditions Observed |
Behavioral | COMT |
Hormones | Oxytocin |
Vasopressin (Antidiuretic Hormone - ADH) | |
Neurological | Dopamine Receptors |
Dopamine Synthesis | |
Dopamine degradation | |
Serotonin Receptors | |
Serotonin Synthesis | |
Serotonin degradation |
Categories | Conditions Observed |
General | Aestuariispira |
Bacteroides_nordii | |
Deltaproteobacteria | |
EscherichiaShigella | |
Klebsiella | |
Klebsiella_variicola | |
Lactivibrio | |
Murimonas | |
Paenibacillus | |
Pelotomaculum | |
Peptoniphilaceae | |
Peptoniphilus | |
Microbiome | Abiotrophy |
Acidaminococcaceae | |
Acidaminococcus | |
Acinetobacter | |
Actinobacteria | |
Actinobacteriaphylum | |
Aestuariispira insulae | |
Aggregatibacter | |
Aggregatibacter actinomycetemcomitans | |
Akkermansia | |
Alistipes shahii | |
Anaerofilum | |
Anaerotruncus | |
Anaerotruncus colihominis | |
Anaerotypes | |
Atopobium | |
Bacilli | |
Bacteroidales | |
Bacteroides | |
Bacteroides caccae | |
Bacteroides dorei | |
Bacteroides thetaiotamicron | |
Bacteroidetes | |
Barnesiellaceae | |
Bifidobacterium | |
Bifidobacterium angulatum | |
Bifidobacterium catenulatum | |
Blautia | |
Blautia coccoides | |
Blautia_glucerasea | |
Blautia_stercoris | |
Blautiagenus | |
Burkholderiales | |
Butyricicoccus Pullicaecorum | |
Butyricimonas | |
Butyricimonas paravirosa | |
Butyricimonas paravirosa | |
Butyricoccus | |
Carnobacteriaceae | |
Choriobacteriaceae | |
Clostridium | |
Clostridium IV | |
Clostridium celerecrescens | |
Clostridium difficile | |
Clostridium xylanovorans | |
Clostridium_cellulolyticum | |
Clostridium_propionicum | |
Coprococcus | |
Coprococcus eats | |
Corynebacterium Jeikeium | |
Cyanobacteria | |
Desulfovibrio | |
Dialister | |
Dialister invisus | |
Dorea | |
Eggerthella | |
Eggerthella sinensis | |
Enterobacteriaceae | |
Erysipelothrix | |
Erysipelotrichaceae family; Erysipelotrichales order; Erysipelotrichia class | |
Erysipelotrichales | |
Erysipelotrichia class, Erysipelotrichales order, Erysipelotrichaceae family | |
Eubacterium | |
Eubacterium Eligens | |
Eubacterium ruminantium | |
Euryarchaeota | |
Faecalibacterium | |
Faecalibacterium prausnitzii | |
Firmicuts | |
Fusobacterium | |
Gammaproteobacteria | |
Gordonibacter | |
Gordonibacter pamelaeae | |
Holdemania | |
Klebsiella variicola | |
Lachnobacterium | |
Lachnospira | |
Lachnospiraceae bacterium 1 1 57FAA | |
Lachnospiraceae noname | |
Lactivibrio alcoholicus | |
Lactobacillales | |
Lactobacillalesorder | |
Lactobacillus | |
Lactobacillus acidophilus | |
Lactococcus lactis | |
Lenta | |
Lentisphaerae | |
Leuconostoc | |
Listipes | |
Marinilabiliaceae | |
Megamonas | |
Megamonas rupelensis | |
Methanobacteriaceae | |
Methanobrevibacter | |
Micrococcaceae | |
Mogibacterium | |
Murimonas intestini | |
Negatives | |
Oscillating | |
Oscillibacter | |
Peptoniphilus Asaccharolyticus | |
Peptostreptococcaceae | |
Phascolarctobacterium | |
Phylum Proteobacteria | |
Porphyromonadaceae | |
Prevotelella | |
Prevotella bivia | |
Pseudobutyrivibrio | |
Rhizobiales | |
Rikenellaceae | |
Rosebury | |
Ruminococcus | |
Ruminococcus flavefaciens | |
Ruminococcus gnavus | |
Ruminococcus obeum | |
S_Clostridium_citroniae.chr1 | |
S_Clostridium_hathewayi.chr12 | |
S_Clostridium_innocuum.chr12 | |
S_Clostridium_symbiosum.chr13 | |
S_Lactococcus_phage_P680.chr11 | |
S_Streptococcus_mutans.chr2 | |
Selenomonadals | |
Slackia | |
Sporacetigenium | |
Streptococcaceae | |
Streptococcus | |
Sutterellaceae | |
Tenericutes | |
Victivalaceae | |
Victivallis | |
Victivallis vadensis | |
Weissella | |
Xylanisolven Bacteroides |
Categories | Conditions Observed |
Need for Nutrients and Metabolism | Choline |
Benefit of Turmeric (Curcumin) | |
Vitamin A | |
Vitamin B1 (Thiamine) | |
B12 vitamin | |
Absorption of Vitamin B12 (FUT2) | |
Vitamin B2 | |
Vitamin B3 (Niacin) | |
Vitamin B5 (Pantothenic Acid) | |
Vitamin B6 | |
Vitamin B7 (Biotin) | |
Vitamin C | |
Vitamin D | |
Vitamin E | |
Vitamin K | |
Benefit of Zeaxanthin | |
Omega 3 | |
Omega 6 | |
Omega 9 | |
Benefit of Betaine | |
Benefit of Bromelain | |
Calcium | |
Copper | |
Coenzyme Q10 | |
Iron | |
Phosphorus | |
Selenium | |
Folate | |
Potassium | |
Deficiency in Fat Metabolism | |
Micronutrient Metabolism | |
Metabolism of Xenobiotics (including caffeine and P-450) | |
Caffeine Metabolization | |
Benefit of Probiotics | |
Lower LDL in Diets Low in Unsaturated Fats | |
Iodine | |
Benefit of Melatonin | |
Body composition | Tendency to Depression |
Slimming with more protein intake than carbohydrates | |
Weight Loss with Carbohydrate Restriction | |
Weight Loss with Calorie Restriction | |
Slimming with more fiber intake | |
Difficulty in Maintaining Weight | |
Thinning with the consumption of complex carbohydrates | |
Slimming with Fat Reduction | |
Preference for bitter foods | |
Preference for sweet foods | |
Preference for fatty foods | |
Tendency to Obesity | |
Tendency to Obesity (monogenic) | |
Mitochondrial Energy Production | |
Tendency to Anxiety | |
Weight gain with saturated fat intake | |
Physical activity | Physical Resistance |
Tendency to Fractures | |
Aerobic Capacity | |
Muscle Strength | |
Muscle Mass Gain | |
Runner with more endurance than speed | |
Pain Tolerance | |
Improved insulin sensitivity with exercise. | |
Imbalances and Deficiencies | Deficiency in the Conversion of T4 to T3 |
Methylenetetrahydrofolate reductase (MTHFR) deficiency | |
L-ferritin Deficiency | |
Tendency to Hyperphagia | |
Collagen Degradation | |
Low Ferritin in Men | |
Low Ferritin in Women | |
Frutosemia | |
Galactosemia | |
Insomnia with Caffeine | |
Sodium reduction to control hypertension | |
Homocysteine Accumulation | |
Platelet Glycoprotein Deficiency IV | |
ALDH2 Deficiency | |
Elastin Deficiency | |
Cholesterol Level (LDL) | |
Mevalonate Kinase Deficiency (MKD) | |
Glucose-6-Phosphate Dehydrogenase Deficiency (G6PD) | |
Growth Hormone Deficiency (GH) | |
Cholesterol Level (HDL) | |
Tendency to Hypertriglyceridemia | |
Response to Antidepressants | |
Autophagy | |
Intolerances and Dysfunctions | Hypercholesterolemia (Type B) |
Hereditary Familial Hypercholesterolemia | |
Hyperparathyroidism | |
Hypothyroidism (Goiter) | |
Type 1 Diabetes | |
Type 2 Diabetes | |
Early Type 2 Diabetes | |
Lower Bone Mineral Density | |
Cow's Milk Allergy | |
Allergy to Egg White | |
Ulcerative Colitis | |
Stroke | |
Acute Myocardial Infarction | |
Acute Myocardial Infarction (early) | |
Cardiac Insufficiency | |
Anorexia Nervosa | |
Lactose Intolerance | |
Gluten Intolerance | |
Colorectal Neoplasia (Meat Consumption) | |
Irritable Bowel Syndrome | |
Metabolic Syndrome | |
Gestational Diabetes | |
Crohn's Disease | |
Gastroesophageal Reflux Disease (GERD) | |
Inflammatory Bowel Disease (IBD) | |
Chronic Kidney Disease (CKD) | |
Autoimmune Thyroid Disease (DTA) | |
Cystic Fibrosis (CF) | |
Hemochromatosis | |
Histamine Intolerance | |
Allergy to Nuts | |
Glutaric Aciduria Type I (AG1) | |
Renal Tubular Acidosis (ATR) | |
Abetalipoproteinemia (Bassen-Kornzweig syndrome) | |
Reduction in Factor XII Activity (Coagulation) | |
Attention Deficit Disorder with Food Dyes | |
Non-Alcoholic Liver Steatosis | |
Alzheimer's Disease | |
Parkinson's Disease | |
Ankylosing Spondylitis | |
Peanut Allergy | |
Alcohol Intolerance | |
Glutamate Intolerance | |
Mercury Intolerance | |
Breast Neoplasm | |
Prostate Neoplasm | |
Lung Neoplasm | |
Inflammation and Oxidative Stress | Need for Detoxification |
Tendency to Oxidative Stress | |
IL-10 | |
IL-1β | |
IL-6 | |
IL-8 | |
IFN-γ | |
TNF |
Categories | Conditions Observed |
Facial Harmonization | Collagen Degradation |
Eyelid sagging | |
Neck sagging | |
Nasogenian Line (Nasolabial Groove) | |
Periocular Lines | |
Perioral Lines | |
Puppet Line | |
Forehead Wrinkles | |
Expression Marks (Glabela) | |
Dark Circles | |
Jowl | |
Volume Loss and Facial Contour | |
Downturned Mouth Corners | |
Permanent Static Wrinkles | |
Nasal Wrinkles | |
Chin Wrinkles | |
Gravitational Wrinkles | |
Collagen Synthesis | |
Hydration Capacity | |
Eyelid Bags | |
Skin Elasticity |
Categories | Conditions Observed |
Joints | Arthrosis of the Knee |
Osteoarthritis | |
Rheumatoid arthritis | |
Hip Osteoarthritis | |
Intestinal Inflammations | Crohn's disease |
Inflammatory Bowel Disease (IBD) | |
Ulcerative Colitis | |
Leaky Bowel Syndrome | |
Gluten Intolerance | |
Lactose intolerance | |
Respiratory | Asthma |
Rhinosinusitis | |
Chronic obstructive pulmonary disease | |
Skin Inflammations | Rosacea |
Atopic Dermatitis | |
Contact dermatitis | |
Brain Inflammation | Parkinson's disease |
Alzheimer's disease | |
Depression | |
Autoinflammatory Diseases | Blau's Syndrome |
Family Periodic Fever | |
Family Mediterranean Fever | |
Familial cold autoinflammatory syndrome (FCAS) | |
Behcet's Disease | |
C-reactive protein | C-reactive protein |
Pro-Inflammatory Cytokines | IL-1 |
IL-1A | |
IL-1B | |
IL-1R | |
IL-1R2 | |
IL-2 | |
IL-2RA | |
IL-2RB | |
IL-2RG | |
IL-6 | |
IL-6R | |
IL-7 | |
IL-8 | |
IL-12 | |
IL-17 | |
IL-17A | |
IL-18 | |
TNF-A | |
Anti-Inflammatory Cytokines | IL-1 |
IL-4 | |
IL-6 | |
IL-10 | |
IL-11 | |
IL-13 | |
IL-19 | |
IL-35 | |
TNF-B | |
IFN-A | |
IFN-G | |
TGF-B | |
MIP2 | |
Chemokines | CCL2 |
CCL3 | |
CCL5 | |
CCL7 | |
CCL8 | |
CCL11 | |
CCL13 | |
CCL17 | |
CCL19 | |
CCL22 | |
CCL25 | |
CCL27 | |
CCR1 | |
CCR2 | |
CCR3 | |
CCR5 | |
CXCR3 | |
CXCR1 | |
CCL2 | |
MIP1A | |
MIP1B | |
MCP1 | |
Hormones and Autoimmune | Testosterone |
Estradiol | |
Hypothyroidism | |
Cortisol Level | |
Others | Rheumatic fever |
Categories | Conditions Observed |
Allergies and Intolerances | Food Allergy |
Food Dye Allergy | |
Peach Allergy | |
Peanut Allergy | |
Milk Allergy | |
Allergy to Nuts and Nuts | |
Allergies in General | |
Histamine intolerance | |
Lactose intolerance | |
Gluten intolerance | |
Hereditary Fructose Intolerance | |
HLA-DQ2.2 | |
HLA-DQ2.5 | |
HLA-DQ4 | |
HLA-DQ7 | |
HLA-DQ8 | |
Pollen Allergy | |
Mite Allergy | |
Asthma | |
Allergic Asthma | |
Reaction to Phthalate | |
Reaction to Bisphenol | |
Nickel Reaction | |
Methylation | Methylation |
COMT | |
Betaine | |
B12 vitamin | |
Vitamin B12 (Levels) | |
Absorption of Vitamin B12 | |
Vitamin B6 | |
Transcobalamin II deficiency | |
ACE | |
MAOA | |
ACAT1 | |
MTR | |
MTRR | |
BHMT | |
AHCY | |
SUOX | |
NOS3 | |
SHMT1 | |
VDR | |
VDR taq rs731236 | |
COMT v158m (mir4761) rs4680 | |
Cellular Energy Production | Mitochondrial Energy Production |
Defect in Carnitine Transport | |
Mitochondrial Biogenesis | |
Primary Carnitine Deficiency | |
Digestive system | Crohn's disease |
Ulcerative Colitis | |
Gastroesophageal Reflux Disease | |
Inflammatory Bowel Disease (IBD) | |
Celiac disease | |
Antioxidants and Detoxification | Oxidative stress |
Glutathione | |
Reaction to Aluminum | |
Lead Reaction | |
Reaction to Mercury | |
Reaction to Arsenic | |
Turmeric (Turmeric) | |
Need for a diet rich in antioxidants | |
Phase II biotransformation | |
Phase I biotransformation | |
Worst oxidative stress with Selenium | |
SULT1A1 gene | |
Detoxification | |
SOD1 | |
SOD2 | |
SOD3 | |
Detox (Detoxification) | |
Folate | Vitamin B9 (Folic Acid) |
Folic Acid Metabolism | |
Folate (Vitamin B9) | |
MTHFR 1298 mutation (rs1801131) | |
Methylenetetrahydrofolate reductase (MTHFR) deficiency | |
Mutation MTHFR 677 (rs1801133) | |
Methionine Cycle | L-methionine |
Methionine Adenosyltransferase Deficiency | |
S-adenosylmethionine (SAMe) | |
Transsulfurization Pathway | Ammonia and Glutamate Production |
CBS gene - Transsulfurization | |
Neurotransmitters | Dopamine Synthesis |
Serotonin Synthesis | |
Dopamine receptors | |
Glutamate Production Factors | |
Degradation of serotonin | |
Conversion of Glutamate to GABA | |
Dopamine conversion | |
DRD2 | |
Noradrenaline | |
Tetrahydrobiopterin | |
Reaction to Glutamate | |
Serotonin receptors | |
Urea, Nitric Oxide and BH4 Cycle | Glutathione Peroxidase-1 mutation |
Mild Hyperphenylalaninemia without BH4 Deficiency | |
BH4 Deficiency Hyperphenylalaninemia | |
Carbamoyl Phosphate Synthesisase Deficiency I | |
Ornithine Transcarbamylase Deficiency | |
Arginine-Succinic Aciduria | |
Citrullinaemia | |
Nitric oxide | |
Argininemia | |
Tetrahydrobiopterin Synthesis Deficiency | |
Metabolism, hormones and detoxification. | Caffeine Metabolization |
Ubiquitins | |
DHEA / DHEAS | |
Fat Metabolism | |
Micronutrient Metabolism | |
Metabolism of Xenobiotics (including caffeine and P-450) | |
Adrenal function | |
Reduction of Hormonal Thyroid Metabolism | |
Risk of Decreased Thyroid Hormone Metabolism | |
Deficiency of Bile Acid Synthesis | |
Hyperthyroidism | |
Protein Metabolization | |
Conversion from T4 to T3 | |
Metabolism of CYP3A4 | |
Adrenocorticotrophic Hormone | |
Insulin resistance | |
Hyperinsulinism | |
Vasopressin | |
Cortisol level | |
Growth Hormone Deficiency (GH) | |
CYP2C19 | |
CYP2C19 * 1 | |
CYP2C19 * 17 | |
Carbohydrate Metabolism | |
Vitamins and Minerals | Vitamin B5 (Pantothenic Acid) |
D vitamin | |
Vitamin B1 (Thiamine) | |
Anacdonic Acid Deficiency | |
GcMAF protein | |
Need for Vitamins | |
Vitamin B7 (Biotin) | |
Copper | |
Vitamin E Deficiency | |
Vitamin E | |
Phosphatidylcholine levels | |
Selenium | |
Coenzyme Q10 | |
Sodium | |
Beta carotene | |
Hemochromatosis | |
Betaine | |
Calcium | |
Choline | |
Magnesium | |
Iron | |
Potassium | |
Vitamin A (Retinol) | |
Vitamin B2 (Riboflavin) | |
Zinc | |
Iodine | |
Hypomagnesemia | |
Low Ferritin | |
Molybdenum | |
Phosphor | |
High Ferritin | |
Vitamin C | |
Vitamin K | |
Vitamin B3 (Niacin) | |
Manganese | |
Molybdenum Cofactor Deficiency | |
Reduced Conversion of Beta Carotene to Retinol | |
Chrome | |
ASD | Autism (delayed onset of speech) |
Autism Spectrum Disorder (ASD) | |
Autism (Asperger's Syndrome) | |
Autism (social communication problem) | |
Growth Delay | |
Motor Development Delay | |
Language Disorder | |
Pyroluria | |
Aggressiveness in children with ADHD | |
Attention Deficit Hyperactivity Disorder (ADHD) | |
Hyperactivity | |
Aggressiveness | |
Anxiety | |
Oppositional-Defiant Disorder (TOD) | |
Obsessive-Compulsive Disorder (OCD) | |
Dyslexia | |
Attention Deficit Disorder with Food Dyes | |
Social Anxiety Disorder (Social Phobia) | |
Seasonal Affective Disorder (SAD) | |
Bipolar Disorder (Response to Lithium Treatment) | |
Bipolar disorder | |
Personality Traits: Hostility, Impulsivity, Anxiety | |
Challenging Behavior | |
Supplementation / Pharmacogenetics | Benefit of Melatonin |
Green Tea Benefit | |
Extrapyramidal Symptom with Risperidone | |
Chamomile | |
Bergamot Oil | |
Natto benefit | |
Benefit of St. John's Wort | |
Resveratrol | |
Zeaxanthin | |
Omega 3 | |
Omega 9 | |
Omega 6 | |
Lutein | |
Bromelain | |
Quercetin | |
Insomnia with Caffeine | |
Reactions with the use of Antidepressants (SSRIs) | |
Passionflower (Vitexin) | |
Response to Fluoxetine (anti-depressant) | |
Response to Hydroxychloroquine | |
Anxiety with Caffeine and Insomnia | |
Personal characteristics | Sense of Taste (Bitter) |
Sense of Taste (Lesser Perception of Salt) | |
Sense of Taste (Sweet) | |
Sense of Taste (Spicy) | |
Misophony | |
Aversion to Coriander | |
Tendency to Overeat (Gluttony) | |
Math Skills | |
Obesity | |
Episodic Memory | |
Memory (verbal) | |
Memory (long term, logic) | |
Musical Aptitude | |
Morning Chronotype | |
Night Chronotype | |
Ephelides (Freckles) | |
Manual dexterity | |
Osphesia | |
Memory | |
Visuospatial Working Memory | |
Motion Sickness | |
Preference for fatty foods | |
Sense of Taste (Umami) | |
Sense of Taste (Sour) | |
Preference for sweet foods | |
Preference for bitter foods | |
Thinness | |
Morning drowsiness | |
Fragmented Sleep | |
Sleep Quality | |
Shortest Sleep Duration | |
Sleep Disorder | |
Microbiota | Clostridium |
Lactobacillus acidophilus | |
Probiotics | |
Family Candidiasis | |
Bifidobacterium | |
Lactobacillus | |
Clostridium difficile | |
Type of muscle fiber | Physical resistance |
Sprinter | |
Endurance | |
Immune system | IgE |
Hyperimmunoglobulin E Syndrome (Hyper IgE) | |
C3 deficiency (immune) | |
T lymphocyte deficiency | |
B Lymphocyte Deficiency | |
Common Variable Immunodeficiency - type 1 | |
Common Variable Immunodeficiency - type 2 | |
Immunodeficiency with Hyper IgM - type 1 | |
Acquired Immune Response | |
Eosinophilic esophagitis | |
Immunodegulation, Polyiendocrinopathy and Enteropathy | |
Severe Combined Immunodeficiency with Sensitivity to Ionizing Radiation | |
Common Variable Immunodeficiency - type 8 | |
Amino Acids | L-arginine |
L-theanine | |
L-lysine | |
L-tyrosine | |
Serine deficiency | |
Susceptibilities Diseases | Anemia |
Sickle Cell Anemia | |
Hemolytic Anemia | |
Microcytic Anemia | |
Homocystinuria-Megaloblastic Anemia | |
Thiamin-Responsive Megaloblastic Anemia | |
Headache | |
Biotinidase deficiency | |
G6PD deficiency | |
Migraine | |
Phenylketonuria | |
Psoriasis | |
Hashimoto's thyroiditis | |
Glutathione Synthesis Deficiency | |
Lyme disease (Borreliosis) | |
Coronavirus 2019 (COVID-19) | |
COVID-19-induced respiratory failure | |
Increased Risk of Intensive Care with COVID-19 | |
Risk of severe COVID-19 | |
Frutosemia | |
L-carnitine deficiency | |
Riboflavin deficiency | |
Depression in Children with Autism | |
Autoimmune disease | |
Autoimmune thyroid disease | |
Schizophrenia | |
Depression | |
Astigmatism | |
Myopia | |
Age-Related Macular Degeneration |
Categories | Conditions Observed |
Other Factors | Waist Measure |
Obesity in Adolescents | |
Obesity | |
Glycation | |
Uric Acid (Concentration) | |
Hypertension (High Blood Pressure) | |
Adiponectin Levels | |
C-reactive protein | |
Polycystic Ovary Syndrome | |
Fasting Glucose Level Increase | |
Less Use of Glucose After Intake of Carbohydrates | |
Quantitative Body Mass Index | |
Decline of NAD | |
Noradrenaline | |
Leptin | |
Resist | |
PI3K | |
AKT | |
PTEN | |
P70S6K | |
GSK3 | |
INSR | |
Wolfram Syndrome 1 | |
Obesity in Type 2 Diabetes Patients | |
Reaction in Cells | ENPP1 |
IRS-1 | |
GLUT4 | |
CAPN10 | |
Lipid Profile | HDL Cholesterol Level |
Cholesterol Level (LDL) | |
Triglycerides | |
Dyslipidemia | |
Diabetes | Type 1 Diabetes |
Type 2 diabetes | |
Early Type 2 Diabetes | |
Insulin Resistance | |
Circulating Glycated Hemoglobin (HbA1c) | |
Impairment of β Cell Function | |
Consequences of Diabetes | Diabetic neuropathy |
Risk of amputation in case of diabetic foot ulcer | |
Diabetic retinopathy | |
Increased Risk of Alzheimer's in Diabetics (T2) | |
Diabetic heart disease ischemic | |
Insulin | Hyperinsulinemia |
Higher Insulin Fasting | |
Hyperinsulinemic Hypoglycemia of Childhood (HHI) | |
Greater Insulin Sensitivity with Physical Exercise | |
Insulinogenic Index | |
Insulin Sensitivity | |
Lower Insulin Secretion | |
Improved Insulin Resistance in Diets with More Protein | |
Pharmacogenetics | Response to Metformin |
Weight Reduction in Liraglutide Treatment | |
GLP-1 | |
DPP-4 |
Categories | Conditions Observed |
MTHFR | MTHFR rs1801131 |
MTHFR rs1801133 |
Categories | Conditions Observed |
Professional | Openness to New Experiences |
Openness to new experiences (Feelings, Actions and Ideas) | |
Increased Environmental Sensitivity | |
Self confidence | |
Ability to Solve Problems | |
Challenging behavior | |
Obsessive behavior | |
Creativity | |
Distrust | |
Disinhibition | |
Manual dexterity | |
Difficulties in Dealing with Criticism | |
Ability to Accept Criticism | |
Cognitive Empathy | |
Entrepreneurship | |
Stress | |
Extroversion | |
Leadership gene | |
Cognitive skills, attention and memory | |
Mathematics Skill | |
Impulsivity | |
Intelligence - IQ | |
Greater learning from mistakes | |
Memory (long term, logic) | |
Opportunism | |
Perfectionism | |
Willingness to avoid mistakes (worse red) | |
Resilience | |
Optimism Trend | |
Decision making with greater risk | |
Statistical Association with Vehicle Accidents | |
Adaptive Capacity | |
Self-discipline at work | |
Cognitive Flexibility | |
Organization | |
Concern for Details | |
Neurological Conditions | Morning Chronotype |
Night chronotype | |
Dyslexia | |
Sleep disorder | |
Motion sickness | |
Hyperactivity | |
Early Wake Up Time | |
Time to sleep later | |
Insomnia | |
Longer Sleep Duration (Greater Need) | |
Greater Stimulus with Caffeine | |
Increased Probability of Fatigue | |
Memory | |
Memory (traumatic) | |
Memory (verbal) | |
Visuospatial Working Memory | |
Episodic memory | |
Less Need for Sleep Hours | |
Oxytocin | |
Tendency to sleep late | |
Type A Personality | |
Type D Personality | |
Neurotransmitters | Dopamine conversion |
Dopamine Synthesis | |
Dopamine receptors | |
Dopamine degradation | |
Dopamine transporters | |
Serotonin degradation | |
Serotonin receptors | |
Serotonin Synthesis | |
Serotonin Transporters | |
Behavioral Conditions | Pleasantness (Acceptability) in Men |
Pleasantness (Acceptability) in Women | |
Happiness | |
Musical Aptitude | |
Lack of sensitivity to children | |
Prosocial behavior | |
Dance | |
Empathy | |
Fear of Uncertainties | |
Lesser Sexual Desire (Female) | |
Loneliness | |
Shame | |
Exploratory Behavior (Novelty Search) | |
Migratory behavior | |
Generosity | |
Fears | |
Sociability | |
Trend of Physical Activity Practice at Leisure | |
Introversion | |
Psychiatric Conditions | Anorexia Nervosa |
Cataplexy and Narcolepsy (sleep) | |
Depression | |
Late dyskinesia | |
Epilepsy | |
Schizophrenia | |
Risk of Depression with Parental Divorce | |
Suicidal tendencies and thoughts | |
Attention Deficit | |
Anxiety | |
Psychiatric Syndromes | Brunner Syndrome |
Panic Syndrome | |
Tourette's Syndrome | |
Personality Traits | Personality Trait: Extraversion |
Personality Trait: Positive Emotions | |
Personality Traits: Hostility, Impulsiveness, Anxiety | |
Personality Trait: Assertiveness | |
Personality Trait: Conscientiousness | |
Personality Trait: Openness, Altruism, Confidence, and Modesty | |
Adictions | Addition to Heroin |
Addition to Tobacco | |
Alcoholism | |
Cocaine addiction | |
Nicotine Dependence | |
Symptoms of Withdrawal in Alcoholism | |
Addiction tendency (gambling, alcohol, smoking) | |
Alcohol Aversion | |
Emotional | Emotional Insensitivity |
Emotional Insecurity | |
Emotional Maturity | |
Emotional Negativity | |
Emotional Vulnerability | |
Relationship Difficulty | |
Conflicts | Aggressiveness |
Aggression with alcohol consumption | |
Antisocial behavior | |
Externalizing Behavior | |
Self-centeredness | |
Indifference | |
Neuroticism | |
Anger | |
Harshness | |
Explosive Temperament | |
Greater Tendency to Lie | |
Disorders | Seasonal Affective Disorder (SAD) |
Bipolar disorder | |
Social Anxiety Disorder (Social Phobia) | |
Binge Eating Disorder | |
Attention Deficit Hyperactivity Disorder (ADHD) | |
Mood Disorder | |
Internalizing Disorder | |
Obsessive-Compulsive Disorder (OCD) | |
Oppositional Defiant Disorder (ODD) | |
Transtorno de Personalidade Borderline |
Categories | Conditions Observed |
Nutrients | Omega 3 |
Omega 6 | |
Hair loss | Loss of hair |
Frontal fibrous alopecia | |
Congenital Universal Alopecia | |
Baldness (Androgenetic Alopecia) | |
Alopecia Areata | |
Women Baldness | |
Male Baldness | |
Calvície Feminina | |
Hair Features | Curly hair |
Thicker hair | |
Straighter hair | |
Red hair | |
White Hair (Earlier Appearance) | |
Pseudofoliculite | |
Structure | Collagen Degradation |
Collagen Synthesis | |
Ceramides | |
Oxidative Stress | Oxidative stress |
Antioxidant Capacity of the Skin | |
Factors of Influence | Stress |
Anxiety | |
Sleep disorder | |
Vitamins | Vitamin B7 (Biotin) |
Vitamin A | |
Vitamin E | |
Vitamin B6 | |
Vitamin C | |
Minerals | Copper |
Zinc | |
Chrome |