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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Categories

Conditions Observed

Cardio-Circulatory SystemAtherosclerosis
 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 SystemMental and Cognitive Decline (Age)
 Stroke
 Alzheimer’s disease
 Parkinson’s disease
 Sleep Quality
 Dopamine Synthesis
 Serotonin Synthesis
  
FertilityMale infertility
  
BehavioralAnxiety
 Seletividade em Relacionamento
 Impulsivity
 Fears
 Mood Disorder
 Depression
 Difficulties in Receiving Reviews
  
Gastrointestinal SystemGluten Intolerance
 Lactose intolerance
 Ulcerative Colitis
 Leaky Gut Syndrome
 Milk Protein Allergy
 Irritable Bowel Syndrome
 Ulcer
 Celiac disease
 Gastritis
  
OncologyThyroid Neoplasm
 Colorectal Neoplasm
 Prostate Neoplasm
 Skin Cancer
 Lungs Cancer
  
Respiratory systemAsthma
 Flu (Influenza)
 Bronchitis
 Apnea
 Pulmonary emphysema
 Allergic Rhinitis
  
Genito-Urinary SystemKidney Calculus
 Benign Prostate Hyperplasia
  
Osteo-Muscular SystemOsteoporosis
 Rheumatoid arthritis
 Arthrosis of the Knee
 Disc herniation
  
Endocrinological System – Disease SusceptibilityMetabolic syndrome
 Autoimmune Thyroid Disease
 Insulin Resistance
 Type 2 diabetes
 Hypothyroidism
  
Endocrinological System – HormonesOxytocin
 Melatonin
 Insulin
 Cortisol
 DHEA/DHEAS
 Progesterone
 Testosterone
 Dihydrotestosterone
  
Sensory SystemCataract
 Age Related Macular Degeneration
 Glaucoma
 Myopia
 Hyperopia
 Astigmatism
 Deafness
  
AllergiesFood Coloring Allergy
 Allergies in General

 

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Conditions observed

Immune systemMTHFR 677 mutation (rs1801133)
 MTHFR 1298 mutation (rs1801131)
 Accumulation of Homocysteine
 Glycation
 Allergies in General
 Allergy to Food Coloring
  
Cardio-Circulatory SystemHigh Ferritin
 Atherosclerosis
 Heart disease
 Hypertension (High Blood Pressure)
 Acute myocardial infarction
 Venous Thrombosis
 Ischemic Stroke
 Cardiac Arrhythmia
 Cholesterol Level (HDL)
 Cholesterol Level (LDL)
 Triglycerides
  
BehavioralDepression
 Relationship Difficulty
 Difficulties in Receiving Reviews
 Impulsivity
 Fears
 Selectivity on Relationships
 Mood Disorder
 Anxiety
  
OncologyThyroid Neoplasm
 Colorectal Neoplasm
 Breast neoplasm
 Ovary Neoplasm
 Endometrial Neoplasm
 Lungs Cancer
 Skin Cancer
  
Osteo-Muscular SystemOsteoporosis
 Rheumatoid arthritis
 Arthrosis of the Knee
 Disc herniation
  
Genito-Urinary SystemKidney Calculus
 Candidiasis
 Polycystic Ovary Syndrome
 Endometriosis
 Uterine Fibroids
 Recurrent Urinary Tract Infection
  
Gastrointestinal SystemCrohn’s disease
 Lactose intolerance
 Ulcerative Colitis
 Leaky Gut Syndrome
 Constipation
 Celiac disease
 Gluten Intolerance
 Irritable bowel syndrome
 Milk Protein Allergy
 Biliary Calculations
 Ulcer
 Gastritis
  
FertilityLower 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 SystemMental and Cognitive Decline (Age)
 Stroke
 Parkinson’s disease
 Sleep Quality
 Dopamine Synthesis
 Serotonin Synthesis
 Alzheimer’s disease
  
Endocrinological System – Disease SusceptibilityHypothyroidism
 Type 2 diabetes
 Metabolic syndrome
 Insulin Resistance
 Hashimoto’s Thyroiditis
  
Endocrinological System – HormonesOxytocin
 Melatonin
 Insulin
 Cortisol
 DHEA/DHEAS
 Testosterone
 Progesterone
 Estradiol
  
Respiratory systemPulmonary emphysema
 Apnea
 Asthma
 Bronchitis
 Flu (Influenza)
 Allergic Rhinitis
  
Sensory SystemCataract
 Age Related Macular Degeneration
 Glaucoma
 Deafness
 Myopia
 Hyperopia
 Astigmatism

 

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Categories

Conditions Observed

AllergiesAllergic 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 systemNon-syndromic deafness
 Otitis
  
Behavioral ChangesAggressiveness
 Neuroticism
  
BenefitsOptimism Trend
  
CancerChildhood Leukemia
 Retinoblastoma
  
CardiovascularAortic stenosis
 Cardiac Arrhythmia
 Cardiovascular Disease (Cholesterol Level)
 Familial Hyperlipoproteinemia Type III
 Hereditary familial hypercholesterolemia
 Hypercholesterolemia (Type B)
  
DentistryCaries
 Periodontitis
 Teeth development
  
DiabetesEarly Type 2 Diabetes
 Type 1 Diabetes
 Type 2 diabetes
  
Digestive systemCanker sores
 Cystic fibrosis
  
Drug ReactionsVaccine Reactions
  
Endocrine systemHashimoto’s Thyroiditis
 Hashimoto’s Thyroiditis (in children)
 Hypothyroidism
  
GeneralAversion to Vegetables and Coffee
 Bacterial Meningitis
 Williams Syndrome
  
Genetic diseasesAngelman 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 systemAnemia
 HDL (Cholesterol)
 Hemolytic Anemia
 Low ferritin in children under 2 years
 Spherocytosis
 Triglycerides
  
HormoneFolic Acid Metabolism
 Growth Hormone (GH) Deficiency
  
HormonesAromatase Deficiency
  
Immune systemAllergy to Food Colors
 Chronic adenoiditis
 HLA-DQ2.2
 HLA-DQ2.5
 HLA-DQ4
 HLA-DQ7
 HLA-DQ8
 Tonsillitis
  
InternalizationsAnxiety
 Depression
 Internalizing Disorder
  
MetabolicCeliac disease
 Lactose intolerance
 Methylenetetrahydrofolate reductase (MTHFR) deficiency
 Obesity
 Trend of Eating Sweets
  
Metabolic disordersCerebrotendinous Xanthomatosis (CTX)
  
Muscular systemBecker Muscular Dystrophy
 Dystonia
  
Need for NutrientsIodine
  
NeurologicalMotor coordination
 Rolandic Epilepsy
 West syndrome
  
PainsHeadache
  
PediatricDelayed Motor Development
 Neonatal Mortality
  
Personal characteristicsAttention 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
  
ProvocativeOppositional defiant disorder (ODD)
  
PsychiatricAddiction 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 systemMale precocious puberty
  
Respiratory systemInterstitial Lung Disease
 Respiratory Syncytial Virus (RSV)
  
Skeletal system (bones)Atelosteogenesis
 Hypochondroplasia
 Musculoskeletal Pain
 Scoliosis
  
SkinAcne
  
Urinary systemChronic Kidney Disease
 Nephroliathiasis in children
 Nephrotic syndrome
 Renal agenesis
 Smaller Kidneys in Newborns
  
Vision (Ophthalmology)Astigmatism
 Myopia
  
VitaminsVitamin D
  
Vitamins needBiotinidase Deficiency
  
WeightBinge Eating Disorder
 Obesity in Adolescents

 

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Conditions Observed

BenefitBenefits of Coffee in Reducing the Risk of Breast Cancer
  
Breast cancerBreast 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
  
CancerCervical 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+)
  
GenesBRCA1
 BRCA2
  
Genetic diseasesHereditary Breast and Ovary Cancer Syndrome
  
HormoneAdiponectin Flag
  
HormonesAromatase Deficiency
 Progesterone
  
OxidationOxidative stress
  
Personal characteristicsTendency to Larger Breasts
 Tendency to have smaller breasts
  
Reactions to TreatmentsBreast Cancer risk associated with estrogen-progesterone combination therapy (EPT)
  
Reproductive systemEndometriosis
 Polycystic Ovary Syndrome
 Uterine Fibroids
 Uterine Fibromyoma

 

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Conditions Observed

AllergiesAllergic 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
  
CardiovascularSensitivity to Vehicle Pollution
  
Genetic diseasesCongenital Ichthyosis
  
Immune systemAllergy to Food Colors
 Food Allergy
 Psoriasis
  
MetabolicCeliac disease
 Gluten Intolerance
 Lactose intolerance
 Sensitivity to Caffeine
  
Metabolic disordersFructosemia
  
Need for NutrientsQuercetin
  
PsychiatricMisophony
 Motion sickness
  
Reactions to TreatmentsGlucocorticoid Resistance
 Glucocorticoid Therapy
  
Respiratory systemAspergillosis
 Rhinosinusitis
  
SkinAlcohol Erythema Reaction
 Erythema
 Histamine
 Ichthyosis
 Inflammatory Skin Response
 Rosacea
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Conditions Observed

Breast cancerDuctal Carcinoma (Breast)
  
CancerOvary Neoplasm
 Testicular Neoplasm
  
CardiovascularProthrombin (G20210A Mutation)
  
Digestive systemConstipation
 Familial Intrahepatic Cholestasis
  
Drug ReactionsCongenital Heart Defect due to Maternal Periconception – SSRIs
 Reactions with the use of antidepressants (SSRI)
  
Endocrine systemHyperthyroidism
 Thyrotoxicosis
 Transient Neonatal Diabetes
  
GeneralLonger Menstrual Cycle Duration
 Menstrual Migraine
  
Hematologic systemCongenital afibrinogenemia
  
Hereditary diseasesFragile X Syndrome
  
HormoneAnti-Müllerian hormone (AMH)
 Dihydrotestosterone (DHT)
 FSH deficiency
 Luteinizing Hormone (LH)
 SHBG levels
  
HormonesEstradiol
 Inhibin
 Isolated Follicle Stimulating Hormone Deficiency (FSH)
 Testosterone
  
Immune systemAnti-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
  
MetabolicCeruloplasmin
  
MethylationMTHFR 1298 mutation (rs1801131)
 MTHFR 677 mutation (rs1801133)
  
PsychiatricPostpartum depression
  
Reproductive systemAzoospermia
 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
  
SkinHereditary Chronic Mucocutaneous Candidiasis
  
Vitamins needRiboflavin Deficiency

 

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Conditions Observed

CancerOral Cavity and Laryngeal Neoplasm
  
DentistryAggressive 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 systemCanker sores
  
Genetic diseasesVan der Woude Syndrome
  
MicrobiomeDialister Species

 

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Conditions Observed

Amino acidsL-arginine
 Serine Deficiency
  
Antioxidants / SupplementsCoenzyme Q10
 Retinoic Acid
  
Auditory systemOtosclerosis
  
Behavioral ChangesAggressiveness
  
CancerGlioma
 Neuroblastoma
  
CardiovascularAtherosclerosis (early in children)
 Atherosclerosis (hyperlipidemia)
 Brain aneurysm
  
Cardiovascular and CerebrovascularNitric Oxide
 Stroke
  
Digestive systemPeroxisomal Enzyme Deficiency
  
Fatty acidsOmega 3
  
Genetic diseasesFamilial 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 systemArgininemia
 Creatinophosphokinase
 Neuroferritinopathy
  
Hereditary diseasesFriedreich’s Ataxia
  
Immune systemGuillain-Barré Syndrome
 Neurofibromatosis
 Neurosarcoidosis
  
InflammationsC-reactive protein
  
MetabolicMitochondrial Complex Deficiency 1
  
Metabolic disordersThiamine 4 Metabolism Dysfunction Syndrome
  
Muscular systemHemiplegia
 Leigh’s Syndrome
  
Need for NutrientsApigenin need
 Choline
 Reaction to Glutamate
 Turmeric (Curcumin)
 Uridine Monophosphate
  
Neurodegenerative diseasesAlzheimer’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
  
NeurologicalBDNF
 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 characteristicsCognitive Flexibility
 Hypothalamus Size (Smaller GG)
 Pineal Hyperplasia
 Visuospatial Working Memory
  
PsychiatricEarly Wake Up Time
 Schizophrenia
  
SleepTime to sleep later
  
VitaminsFolate
 Vitamin B3 (Niacin)
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Conditions Observed

Amino acidsN-acetylcysteine
  
Antioxidants / SupplementsCoenzyme Q10
 Glutathione
 Probiotics
 Retinol
  
BenefitBenefit of Green Tea
 Chamomile
 Passionflower (Vitexin)
 S-adenosylmethionine (SAMe)
  
Cardiovascular and CerebrovascularNitric Oxide
  
Essential Amino AcidsL-methionine
  
Fatty acidsOmega 3
 Omega 6
 Omega 9
  
HormonesBenefit of Melatonin
 DHEA/DHEAS
  
MetabolicSerum Ascorbate Levels
  
Metabolic disordersHyperferritinemia
  
MineralsBlood Phosphate Levels
  
Need for NutrientsApigenin
 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
  
VitaminsBeta 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 needRiboflavin Deficiency

 

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Categories

Conditions Observed

CancerBiliary 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
  
CardiovascularArginine-succinic aciduria
  
Digestive systemABCB1 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 ReactionsHepatitis caused by anti-tuberculosis drugs
  
GeneralALT / AST Index
 Hepatocellular Carcinoma (HCC)
 Protein Digestive Capacity
  
Genetic diseasesAlpha-1 Antitrypsin Deficiency
 Hereditary angioedema
 Mucolipidosis Type 4 (Gangliosidosis)
 Peutz-Jeghers syndrome
 Primary Hyperoxaluria
 Wilson’s Disease
 Zellweger Syndrome
  
Hematologic systemAlbumin
 Aspartate Aminotransferase (AST)
 Haptoglobin
 Hemochromatosis
 High Ferritin
 Hyperbilirubinemia
 Low Ferritin in Men
 Low Ferritin in Women
 Transferrin
  
Immune systemCrohn’s disease
 HLA-DQ2.2
 HLA-DQ2.5
 HLA-DQ4
 HLA-DQ7
 HLA-DQ8
 Primary Sclerosing Cholangitis
  
InflammationsInflammatory Bowel Disease (IBD)
 Sarcoidosis
 Yao’s Syndrome
  
MetabolicCeliac disease
 Ceruloplasmin
 Gluten Intolerance
 Lactose intolerance
 Lipid Metabolism
 Sensitivity to Caffeine
  
Metabolic disordersGlycogen Storage Disease
 Hyperferritinemia
 Low Ferritin
 Methylmalonic Acidemia
 Niacin’s Benefit in Reducing Liver Fat
 Niemann-Pick Disease
  
Need for NutrientsMolybdenum
  
Reactions to TreatmentsBenefit of Aspirin on colorectal cancer risk
 Glucocorticoid Resistance
 Glucocorticoid Therapy
  
Urinary systemFocal Segmental Glomerulosclerosis
 Risk of formation of Gallstones
  
VitaminsVitamin B12 (Levels)
  
WeightBinge Eating Disorder
 Reduction of body fat with intervention of polyphenols

 

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Categories

Conditions Observed

Breast cancerBreast Neoplasm (Family)
 Breast neoplasm
 Ductal Carcinoma (Breast)
  
CancerAcute 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 systemBowel polyps
 Juvenile Polyposis Syndrome
  
Drug ReactionsRisk of Peripheral Neuropathy using Taxane
  
GeneralHepatocellular Carcinoma (HCC)
  
GenesGSTT1
  
Genetic diseasesBloom Syndrome
 Hereditary Breast and Ovary Cancer Syndrome
 Peutz-Jeghers syndrome
 Proteus Syndrome
 Rasopathies
  
Hematologic systemIdiopathic Hypereosinophilic Syndrome
  
HormoneAdiponectin Flag
  
Immune systemNeurofibromatosis
  
Neurodegenerative diseasesLouis-Bar Syndrome (Ataxia Telangiectasia)
  
OncologicBRAF V600E mutation
 Choroidal Melanoma
  
Reactions to TreatmentsAllogeneic Rejection
 Benefit of Aspirin on colorectal cancer risk
 Camel Milk Benefit in Smokers
 Chemotherapy Effectiveness
 Fluoroucacil Response
 Glucocorticoid Resistance
 Glucocorticoid Therapy
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Categories

Conditions Observed

Amino acidsBeta-alanine
 L-carnitine Deficiency
 L-glutamine
 Monohydrate Creatine
  
Antioxidants / SupplementsBCAA levels
 Beta-Casein A1
 Beta-Casein A2A2
 Leucine Absorption
 Retinoic Acid
 Vegetarian Protein Shake
 Whey Protein
  
BehaviorsMotivation to Exercise
 Persistence
 Sports Behavior
  
BenefitsAdaptability
  
CardiovascularAerobic 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 acidsArachidonic Acid Deficiency
  
GeneralCanoeing
 Protein Digestive Capacity
  
Genetic diseasesSudden Death Syndrome
 Walker-Warburg Syndrome
  
Hematologic systemBenefit of Physical Exercise for HDL
 High Ferritin
  
Hereditary diseasesPompe disease
  
HormonesCortisol Level
 DHEA/DHEAS
 Increased Cortisol (in women)
 Increased Noradrenaline Level During Exercise
 Progesterone
 Suppression of the secretion of luteinizing hormone due to anabolics
 Testosterone
  
InjuriesAchilles 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
  
MetabolicGreater 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 systemAchilles 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
  
NeurologicalMotor coordination
  
PainsBack pains
 Lumbar Disc Disease
 Pain Sensitivity
  
Personal characteristicsAbility 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
  
ProvocativeChallenging behavior
  
PsychiatricAddiction tendency (eating, gambling, alcohol, smoking)
 Disinhibition
  
Reasons for ConflictDifficulties in Dealing with Criticism
  
Respiratory systemAerobic 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
  
Sports100/200/400m 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
  
VitaminsVitamin B2
 Vitamin B6
 Vitamin B9 (Folic Acid)
  
WeightBenefit 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

 

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Categories

Conditions Observed

Antioxidants / SupplementsGlutathione
 Primary Carnitine Deficiency
  
Breast cancerBreast Neoplasm (Family)
 Breast neoplasm
  
CancerColon Neoplasm
 Colorectal Neoplasm
 Colorectal Neoplasm (Family)
 Endometrial Neoplasm
 Hereditary Nonpolyposis Colorectal Neoplasm
 Ovary Neoplasm
  
CardiovascularProthrombin (G20210A Mutation)
 Ventricular Tachycardia
  
DentistryCleft lip
  
DiabetesType 1 Diabetes
  
Digestive systemIrritable Bowel Syndrome
  
Drug ReactionsCongenital Heart Defect due to Maternal Periconception – SSRIs
  
Endocrine systemTransient Neonatal Diabetes
  
GeneralLonger Menstrual Cycle Duration
 Menstrual Migraine
  
Genetic diseasesHereditary Breast and Ovary Cancer Syndrome
 Primary Autosomal Microcephaly
 Primary Microcephaly
  
Hematologic systemCongenital afibrinogenemia
 Factor VII Deficiency
 Hereditary Persistence of Fetal Hemoglobin (HPFH)
  
Hereditary diseasesFragile X Syndrome
  
HormoneFSH deficiency
  
HormonesAromatase Deficiency
 DHEA/DHEAS
 Estradiol
 Estriol
 Estrone
 Isolated Follicle Stimulating Hormone Deficiency (FSH)
 Oxytocin
 Progesterone
  
Immune systemAnti-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
  
InflammationsSjogren’s Syndrome
  
MetabolicGlucose-6-Phosphate Dehydrogenase (G6PD) Deficiency
 Weight Gain Trend
  
MethylationMTHFR 1298 mutation (rs1801131)
 MTHFR 677 mutation (rs1801133)
  
Muscular systemHemiplegia
  
Need for NutrientsIron
  
PediatricNeonatal Seizure Disorders
  
Personal characteristicsGonadal dysgenesis
  
Reactions to TreatmentsAllogeneic Rejection
  
Reproductive systemAge 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
  
SkinJaundice
 Keloids
 Varicose veins
  
Urinary systemRecurrent Urinary Infection
 Urinary incontinence
  
VitaminsFolate
 Vitamin A
 Vitamin B12
 Vitamin B6
 Vitamin B9 (Folic Acid)
 Vitamin C
 Vitamin D
 Vitamin E
 Vitamin K

 

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Categories

Conditions

Auditory systemUsher Syndrome
  
CancerBAP1 – Tumor Predisposition Syndrome
 Retinoblastoma
 Tumor predisposition syndrome (BAP1)
  
DiabetesType 1 Diabetes
 Type 2 diabetes
  
Genetic diseasesAlport’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 systemCongenital Erythropoietic Porphyria (Gunther’s Disease)
 Graves’ Disease
 HLA-DQ4
  
InflammationsPresence of the HLA-B27 Allele
 Sjogren’s Syndrome
 Uveitis
  
MetabolicGlycation
 Methylenetetrahydrofolate reductase (MTHFR) deficiency
  
Metabolic disordersHomocystinuria
 Hyperferritinemia
 Hypoalphalipoproteinemia (Tangier’s Disease)
  
Muscular systemLeigh’s Syndrome
 Muscular Dystrophy – Congenital Dystroglycanopathy
  
Need for NutrientsLutein
 Zeaxanthin
  
Neurodegenerative diseasesProgressive Supranuclear Palsy
  
OncologicChoroidal Melanoma
  
Personal characteristicsDouble eyelids
  
Reactions to TreatmentsAllogeneic Rejection
 Glucocorticoid Resistance
 Glucocorticoid Therapy
  
SkinBasal 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
  
VitaminsBeta carotene
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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

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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

 

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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
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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)
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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
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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
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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

 

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Categories

Conditions Observed

Behavioral

COMT

Hormones

Oxytocin
Vasopressin (Antidiuretic Hormone – ADH)

 

Neurological

Dopamine Receptors
Dopamine Synthesis
Dopamine degradation
Serotonin Receptors
Serotonin Synthesis
Serotonin degradation
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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
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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
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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
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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
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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
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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
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Conditions Observed

MTHFR

MTHFR rs1801131
MTHFR rs1801133
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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
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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 SystemAtherosclerosis
 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 SystemMental and Cognitive Decline (Age)
 Stroke
 Alzheimer's disease
 Parkinson's disease
 Sleep Quality
 Dopamine Synthesis
 Serotonin Synthesis
  
FertilityMale infertility
  
BehavioralAnxiety
 Seletividade em Relacionamento
 Impulsivity
 Fears
 Mood Disorder
 Depression
 Difficulties in Receiving Reviews
  
Gastrointestinal SystemGluten Intolerance
 Lactose intolerance
 Ulcerative Colitis
 Leaky Gut Syndrome
 Milk Protein Allergy
 Irritable Bowel Syndrome
 Ulcer
 Celiac disease
 Gastritis
  
OncologyThyroid Neoplasm
 Colorectal Neoplasm
 Prostate Neoplasm
 Skin Cancer
 Lungs Cancer
  
Respiratory systemAsthma
 Flu (Influenza)
 Bronchitis
 Apnea
 Pulmonary emphysema
 Allergic Rhinitis
  
Genito-Urinary SystemKidney Calculus
 Benign Prostate Hyperplasia
  
Osteo-Muscular SystemOsteoporosis
 Rheumatoid arthritis
 Arthrosis of the Knee
 Disc herniation
  
Endocrinological System - Disease SusceptibilityMetabolic syndrome
 Autoimmune Thyroid Disease
 Insulin Resistance
 Type 2 diabetes
 Hypothyroidism
  
Endocrinological System - HormonesOxytocin
 Melatonin
 Insulin
 Cortisol
 DHEA/DHEAS
 Progesterone
 Testosterone
 Dihydrotestosterone
  
Sensory SystemCataract
 Age Related Macular Degeneration
 Glaucoma
 Myopia
 Hyperopia
 Astigmatism
 Deafness
  
AllergiesFood Coloring Allergy
 Allergies in General

CategoriesConditions Observed
Immune systemMTHFR 677 mutation (rs1801133)
 MTHFR 1298 mutation (rs1801131)
 Accumulation of Homocysteine
 Glycation
 Allergies in General
 Allergy to Food Coloring
  
Cardio-Circulatory SystemHigh Ferritin
 Atherosclerosis
 Heart disease
 Hypertension (High Blood Pressure)
 Acute myocardial infarction
 Venous Thrombosis
 Ischemic Stroke
 Cardiac Arrhythmia
 Cholesterol Level (HDL)
 Cholesterol Level (LDL)
 Triglycerides
  
BehavioralDepression
 Relationship Difficulty
 Difficulties in Receiving Reviews
 Impulsivity
 Fears
 Selectivity on Relationships
 Mood Disorder
 Anxiety
  
OncologyThyroid Neoplasm
 Colorectal Neoplasm
 Breast neoplasm
 Ovary Neoplasm
 Endometrial Neoplasm
 Lungs Cancer
 Skin Cancer
  
Osteo-Muscular SystemOsteoporosis
 Rheumatoid arthritis
 Arthrosis of the Knee
 Disc herniation
  
Genito-Urinary SystemKidney Calculus
 Candidiasis
 Polycystic Ovary Syndrome
 Endometriosis
 Uterine Fibroids
 Recurrent Urinary Tract Infection
  
Gastrointestinal SystemCrohn's disease
 Lactose intolerance
 Ulcerative Colitis
 Leaky Gut Syndrome
 Constipation
 Celiac disease
 Gluten Intolerance
 Irritable bowel syndrome
 Milk Protein Allergy
 Biliary Calculations
 Ulcer
 Gastritis
  
FertilityLower 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 SystemMental and Cognitive Decline (Age)
 Stroke
 Parkinson's disease
 Sleep Quality
 Dopamine Synthesis
 Serotonin Synthesis
 Alzheimer's disease
  
Endocrinological System - Disease SusceptibilityHypothyroidism
 Type 2 diabetes
 Metabolic syndrome
 Insulin Resistance
 Hashimoto's Thyroiditis
  
Endocrinological System - HormonesOxytocin
 Melatonin
 Insulin
 Cortisol
 DHEA/DHEAS
 Testosterone
 Progesterone
 Estradiol
  
Respiratory systemPulmonary emphysema
 Apnea
 Asthma
 Bronchitis
 Flu (Influenza)
 Allergic Rhinitis
  
Sensory SystemCataract
 Age Related Macular Degeneration
 Glaucoma
 Deafness
 Myopia
 Hyperopia
 Astigmatism
CategoriesConditions Observed
AllergiesAllergic 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 systemNon-syndromic deafness
 Otitis
  
Behavioral ChangesAggressiveness
 Neuroticism
  
BenefitsOptimism Trend
  
CancerChildhood Leukemia
 Retinoblastoma
  
CardiovascularAortic stenosis
 Cardiac Arrhythmia
 Cardiovascular Disease (Cholesterol Level)
 Familial Hyperlipoproteinemia Type III
 Hereditary familial hypercholesterolemia
 Hypercholesterolemia (Type B)
  
DentistryCaries
 Periodontitis
 Teeth development
  
DiabetesEarly Type 2 Diabetes
 Type 1 Diabetes
 Type 2 diabetes
  
Digestive systemCanker sores
 Cystic fibrosis
  
Drug ReactionsVaccine Reactions
  
Endocrine systemHashimoto's Thyroiditis
 Hashimoto's Thyroiditis (in children)
 Hypothyroidism
  
GeneralAversion to Vegetables and Coffee
 Bacterial Meningitis
 Williams Syndrome
  
Genetic diseasesAngelman 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 systemAnemia
 HDL (Cholesterol)
 Hemolytic Anemia
 Low ferritin in children under 2 years
 Spherocytosis
 Triglycerides
  
HormoneFolic Acid Metabolism
 Growth Hormone (GH) Deficiency
  
HormonesAromatase Deficiency
  
Immune systemAllergy to Food Colors
 Chronic adenoiditis
 HLA-DQ2.2
 HLA-DQ2.5
 HLA-DQ4
 HLA-DQ7
 HLA-DQ8
 Tonsillitis
  
InternalizationsAnxiety
 Depression
 Internalizing Disorder
  
MetabolicCeliac disease
 Lactose intolerance
 Methylenetetrahydrofolate reductase (MTHFR) deficiency
 Obesity
 Trend of Eating Sweets
  
Metabolic disordersCerebrotendinous Xanthomatosis (CTX)
  
Muscular systemBecker Muscular Dystrophy
 Dystonia
  
Need for NutrientsIodine
  
NeurologicalMotor coordination
 Rolandic Epilepsy
 West syndrome
  
PainsHeadache
  
PediatricDelayed Motor Development
 Neonatal Mortality
  
Personal characteristicsAttention 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
  
ProvocativeOppositional defiant disorder (ODD)
  
PsychiatricAddiction 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 systemMale precocious puberty
  
Respiratory systemInterstitial Lung Disease
 Respiratory Syncytial Virus (RSV)
  
Skeletal system (bones)Atelosteogenesis
 Hypochondroplasia
 Musculoskeletal Pain
 Scoliosis
  
SkinAcne
  
Urinary systemChronic Kidney Disease
 Nephroliathiasis in children
 Nephrotic syndrome
 Renal agenesis
 Smaller Kidneys in Newborns
  
Vision (Ophthalmology)Astigmatism
 Myopia
  
VitaminsVitamin D
  
Vitamins needBiotinidase Deficiency
  
WeightBinge Eating Disorder
 Obesity in Adolescents
CategoriesConditions Observed
BenefitBenefits of Coffee in Reducing the Risk of Breast Cancer
  
Breast cancerBreast 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
  
CancerCervical 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+)
  
GenesBRCA1
 BRCA2
  
Genetic diseasesHereditary Breast and Ovary Cancer Syndrome
  
HormoneAdiponectin Flag
  
HormonesAromatase Deficiency
 Progesterone
  
OxidationOxidative stress
  
Personal characteristicsTendency to Larger Breasts
 Tendency to have smaller breasts
  
Reactions to TreatmentsBreast Cancer risk associated with estrogen-progesterone combination therapy (EPT)
  
Reproductive systemEndometriosis
 Polycystic Ovary Syndrome
 Uterine Fibroids
 Uterine Fibromyoma
CategoriesConditions Observed
AllergiesAllergic 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
  
CardiovascularSensitivity to Vehicle Pollution
  
Genetic diseasesCongenital Ichthyosis
  
Immune systemAllergy to Food Colors
 Food Allergy
 Psoriasis
  
MetabolicCeliac disease
 Gluten Intolerance
 Lactose intolerance
 Sensitivity to Caffeine
  
Metabolic disordersFructosemia
  
Need for NutrientsQuercetin
  
PsychiatricMisophony
 Motion sickness
  
Reactions to TreatmentsGlucocorticoid Resistance
 Glucocorticoid Therapy
  
Respiratory systemAspergillosis
 Rhinosinusitis
  
SkinAlcohol Erythema Reaction
 Erythema
 Histamine
 Ichthyosis
 Inflammatory Skin Response
 Rosacea

Categories

Conditions Observed
Breast cancerDuctal Carcinoma (Breast)
  
CancerOvary Neoplasm
 Testicular Neoplasm
  
CardiovascularProthrombin (G20210A Mutation)
  
Digestive systemConstipation
 Familial Intrahepatic Cholestasis
  
Drug ReactionsCongenital Heart Defect due to Maternal Periconception - SSRIs
 Reactions with the use of antidepressants (SSRI)
  
Endocrine systemHyperthyroidism
 Thyrotoxicosis
 Transient Neonatal Diabetes
  
GeneralLonger Menstrual Cycle Duration
 Menstrual Migraine
  
Hematologic systemCongenital afibrinogenemia
  
Hereditary diseasesFragile X Syndrome
  
HormoneAnti-Müllerian hormone (AMH)
 Dihydrotestosterone (DHT)
 FSH deficiency
 Luteinizing Hormone (LH)
 SHBG levels
  
HormonesEstradiol
 Inhibin
 Isolated Follicle Stimulating Hormone Deficiency (FSH)
 Testosterone
  
Immune systemAnti-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
  
MetabolicCeruloplasmin
  
MethylationMTHFR 1298 mutation (rs1801131)
 MTHFR 677 mutation (rs1801133)
  
PsychiatricPostpartum depression
  
Reproductive systemAzoospermia
 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
  
SkinHereditary Chronic Mucocutaneous Candidiasis
  
Vitamins needRiboflavin Deficiency

 

CategoriesConditions Observed
CancerOral Cavity and Laryngeal Neoplasm
  
DentistryAggressive 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 systemCanker sores
  
Genetic diseasesVan der Woude Syndrome
  
MicrobiomeDialister Species

 

CategoriesConditions Observed
Amino acidsL-arginine
 Serine Deficiency
  
Antioxidants / SupplementsCoenzyme Q10
 Retinoic Acid
  
Auditory systemOtosclerosis
  
Behavioral ChangesAggressiveness
  
CancerGlioma
 Neuroblastoma
  
CardiovascularAtherosclerosis (early in children)
 Atherosclerosis (hyperlipidemia)
 Brain aneurysm
  
Cardiovascular and CerebrovascularNitric Oxide
 Stroke
  
Digestive systemPeroxisomal Enzyme Deficiency
  
Fatty acidsOmega 3
  
Genetic diseasesFamilial 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 systemArgininemia
 Creatinophosphokinase
 Neuroferritinopathy
  
Hereditary diseasesFriedreich's Ataxia
  
Immune systemGuillain-Barré Syndrome
 Neurofibromatosis
 Neurosarcoidosis
  
InflammationsC-reactive protein
  
MetabolicMitochondrial Complex Deficiency 1
  
Metabolic disordersThiamine 4 Metabolism Dysfunction Syndrome
  
Muscular systemHemiplegia
 Leigh's Syndrome
  
Need for NutrientsApigenin need
 Choline
 Reaction to Glutamate
 Turmeric (Curcumin)
 Uridine Monophosphate
  
Neurodegenerative diseasesAlzheimer'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
  
NeurologicalBDNF
 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 characteristicsCognitive Flexibility
 Hypothalamus Size (Smaller GG)
 Pineal Hyperplasia
 Visuospatial Working Memory
  
PsychiatricEarly Wake Up Time
 Schizophrenia
  
SleepTime to sleep later
  
VitaminsFolate
 Vitamin B3 (Niacin)

 

CategoriesConditions Observed
Amino acidsN-acetylcysteine
  
Antioxidants / SupplementsCoenzyme Q10
 Glutathione
 Probiotics
 Retinol
  
BenefitBenefit of Green Tea
 Chamomile
 Passionflower (Vitexin)
 S-adenosylmethionine (SAMe)
  
Cardiovascular and CerebrovascularNitric Oxide
  
Essential Amino AcidsL-methionine
  
Fatty acidsOmega 3
 Omega 6
 Omega 9
  
HormonesBenefit of Melatonin
 DHEA/DHEAS
  
MetabolicSerum Ascorbate Levels
  
Metabolic disordersHyperferritinemia
  
MineralsBlood Phosphate Levels
  
Need for NutrientsApigenin
 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
  
VitaminsBeta 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 needRiboflavin Deficiency

 

CategoriesConditions Observed
CancerBiliary 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
  
CardiovascularArginine-succinic aciduria
  
Digestive systemABCB1 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 ReactionsHepatitis caused by anti-tuberculosis drugs
  
GeneralALT / AST Index
 Hepatocellular Carcinoma (HCC)
 Protein Digestive Capacity
  
Genetic diseasesAlpha-1 Antitrypsin Deficiency
 Hereditary angioedema
 Mucolipidosis Type 4 (Gangliosidosis)
 Peutz-Jeghers syndrome
 Primary Hyperoxaluria
 Wilson's Disease
 Zellweger Syndrome
  
Hematologic systemAlbumin
 Aspartate Aminotransferase (AST)
 Haptoglobin
 Hemochromatosis
 High Ferritin
 Hyperbilirubinemia
 Low Ferritin in Men
 Low Ferritin in Women
 Transferrin
  
Immune systemCrohn's disease
 HLA-DQ2.2
 HLA-DQ2.5
 HLA-DQ4
 HLA-DQ7
 HLA-DQ8
 Primary Sclerosing Cholangitis
  
InflammationsInflammatory Bowel Disease (IBD)
 Sarcoidosis
 Yao's Syndrome
  
MetabolicCeliac disease
 Ceruloplasmin
 Gluten Intolerance
 Lactose intolerance
 Lipid Metabolism
 Sensitivity to Caffeine
  
Metabolic disordersGlycogen Storage Disease
 Hyperferritinemia
 Low Ferritin
 Methylmalonic Acidemia
 Niacin's Benefit in Reducing Liver Fat
 Niemann-Pick Disease
  
Need for NutrientsMolybdenum
  
Reactions to TreatmentsBenefit of Aspirin on colorectal cancer risk
 Glucocorticoid Resistance
 Glucocorticoid Therapy
  
Urinary systemFocal Segmental Glomerulosclerosis
 Risk of formation of Gallstones
  
VitaminsVitamin B12 (Levels)
  
WeightBinge Eating Disorder
 Reduction of body fat with intervention of polyphenols

 

CategoriesConditions Observed
Breast cancerBreast Neoplasm (Family)
 Breast neoplasm
 Ductal Carcinoma (Breast)
  
CancerAcute 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 systemBowel polyps
 Juvenile Polyposis Syndrome
  
Drug ReactionsRisk of Peripheral Neuropathy using Taxane
  
GeneralHepatocellular Carcinoma (HCC)
  
GenesGSTT1
  
Genetic diseasesBloom Syndrome
 Hereditary Breast and Ovary Cancer Syndrome
 Peutz-Jeghers syndrome
 Proteus Syndrome
 Rasopathies
  
Hematologic systemIdiopathic Hypereosinophilic Syndrome
  
HormoneAdiponectin Flag
  
Immune systemNeurofibromatosis
  
Neurodegenerative diseasesLouis-Bar Syndrome (Ataxia Telangiectasia)
  
OncologicBRAF V600E mutation
 Choroidal Melanoma
  
Reactions to TreatmentsAllogeneic Rejection
 Benefit of Aspirin on colorectal cancer risk
 Camel Milk Benefit in Smokers
 Chemotherapy Effectiveness
 Fluoroucacil Response
 Glucocorticoid Resistance
 Glucocorticoid Therapy

CategoriesConditions Observed
Amino acidsBeta-alanine
 L-carnitine Deficiency
 L-glutamine
 Monohydrate Creatine
  
Antioxidants / SupplementsBCAA levels
 Beta-Casein A1
 Beta-Casein A2A2
 Leucine Absorption
 Retinoic Acid
 Vegetarian Protein Shake
 Whey Protein
  
BehaviorsMotivation to Exercise
 Persistence
 Sports Behavior
  
BenefitsAdaptability
  
CardiovascularAerobic 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 acidsArachidonic Acid Deficiency
  
GeneralCanoeing
 Protein Digestive Capacity
  
Genetic diseasesSudden Death Syndrome
 Walker-Warburg Syndrome
  
Hematologic systemBenefit of Physical Exercise for HDL
 High Ferritin
  
Hereditary diseasesPompe disease
  
HormonesCortisol Level
 DHEA/DHEAS
 Increased Cortisol (in women)
 Increased Noradrenaline Level During Exercise
 Progesterone
 Suppression of the secretion of luteinizing hormone due to anabolics
 Testosterone
  
InjuriesAchilles 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
  
MetabolicGreater 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 systemAchilles 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
  
NeurologicalMotor coordination
  
PainsBack pains
 Lumbar Disc Disease
 Pain Sensitivity
  
Personal characteristicsAbility 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
  
ProvocativeChallenging behavior
  
PsychiatricAddiction tendency (eating, gambling, alcohol, smoking)
 Disinhibition
  
Reasons for ConflictDifficulties in Dealing with Criticism
  
Respiratory systemAerobic 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
  
Sports100/200/400m 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
  
VitaminsVitamin B2
 Vitamin B6
 Vitamin B9 (Folic Acid)
  
WeightBenefit 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
CategoriesConditions Observed
Antioxidants / SupplementsGlutathione
 Primary Carnitine Deficiency
  
Breast cancerBreast Neoplasm (Family)
 Breast neoplasm
  
CancerColon Neoplasm
 Colorectal Neoplasm
 Colorectal Neoplasm (Family)
 Endometrial Neoplasm
 Hereditary Nonpolyposis Colorectal Neoplasm
 Ovary Neoplasm
  
CardiovascularProthrombin (G20210A Mutation)
 Ventricular Tachycardia
  
DentistryCleft lip
  
DiabetesType 1 Diabetes
  
Digestive systemIrritable Bowel Syndrome
  
Drug ReactionsCongenital Heart Defect due to Maternal Periconception - SSRIs
  
Endocrine systemTransient Neonatal Diabetes
  
GeneralLonger Menstrual Cycle Duration
 Menstrual Migraine
  
Genetic diseasesHereditary Breast and Ovary Cancer Syndrome
 Primary Autosomal Microcephaly
 Primary Microcephaly
  
Hematologic systemCongenital afibrinogenemia
 Factor VII Deficiency
 Hereditary Persistence of Fetal Hemoglobin (HPFH)
  
Hereditary diseasesFragile X Syndrome
  
HormoneFSH deficiency
  
HormonesAromatase Deficiency
 DHEA/DHEAS
 Estradiol
 Estriol
 Estrone
 Isolated Follicle Stimulating Hormone Deficiency (FSH)
 Oxytocin
 Progesterone
  
Immune systemAnti-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
  
InflammationsSjogren's Syndrome
  
MetabolicGlucose-6-Phosphate Dehydrogenase (G6PD) Deficiency
 Weight Gain Trend
  
MethylationMTHFR 1298 mutation (rs1801131)
 MTHFR 677 mutation (rs1801133)
  
Muscular systemHemiplegia
  
Need for NutrientsIron
  
PediatricNeonatal Seizure Disorders
  
Personal characteristicsGonadal dysgenesis
  
Reactions to TreatmentsAllogeneic Rejection
  
Reproductive systemAge 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
  
SkinJaundice
 Keloids
 Varicose veins
  
Urinary systemRecurrent Urinary Infection
 Urinary incontinence
  
VitaminsFolate
 Vitamin A
 Vitamin B12
 Vitamin B6
 Vitamin B9 (Folic Acid)
 Vitamin C
 Vitamin D
 Vitamin E
 Vitamin K
CategoriesConditions Observed
Auditory systemUsher Syndrome
  
CancerBAP1 - Tumor Predisposition Syndrome
 Retinoblastoma
 Tumor predisposition syndrome (BAP1)
  
DiabetesType 1 Diabetes
 Type 2 diabetes
  
Genetic diseasesAlport'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 systemCongenital Erythropoietic Porphyria (Gunther's Disease)
 Graves' Disease
 HLA-DQ4
  
InflammationsPresence of the HLA-B27 Allele
 Sjogren's Syndrome
 Uveitis
  
MetabolicGlycation
 Methylenetetrahydrofolate reductase (MTHFR) deficiency
  
Metabolic disordersHomocystinuria
 Hyperferritinemia
 Hypoalphalipoproteinemia (Tangier's Disease)
  
Muscular systemLeigh's Syndrome
 Muscular Dystrophy - Congenital Dystroglycanopathy
  
Need for NutrientsLutein
 Zeaxanthin
  
Neurodegenerative diseasesProgressive Supranuclear Palsy
  
OncologicChoroidal Melanoma
  
Personal characteristicsDouble eyelids
  
Reactions to TreatmentsAllogeneic Rejection
 Glucocorticoid Resistance
 Glucocorticoid Therapy
  
SkinBasal 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
  
VitaminsBeta carotene
CategoriesConditions Observed
AgingAging (quality)
 Facial Age and Appearance (greater aging)
 Telomere shortening
  
AllergiesAllergies 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 acidsL-arginine
  
Antioxidants / SupplementsCoenzyme Q10
  
CancerBAP1 - 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 systemCanker sores
  
Fatty acidsOmega 3
 Omega 6
 Omega 9
  
GeneralLoss of hair
  
Genetic diseasesBart-Pumphrey Syndrome
 Blau's Syndrome
 Cardio-facio-cutaneous syndrome
 Elastic pseudoxanthoma
 Hereditary angioedema
 Hypohydrotic Ectodermal Dysplasia
 Ictiosis Vulgaris
 Oculocutaneous Albinism
 Proteus Syndrome
  
Hematologic systemHyperbilirubinemia
 Post-Transfusion Purpura (PPT)
  
Immune systemCongenital Erythropoietic Porphyria (Gunther's Disease)
 Dermatomyositis
 Herpes
 Lichen Planus
 Psoriasis
  
InflammationsBehçet's Disease
 Frontal Fibrosing Alopecia
 Sarcoidosis
 Scleroderma
 Sjogren's Syndrome
  
MetabolicGlycation
  
Metabolic disordersAcute Intermittent Porphyria
 Lipodystrophy
 Variegate Porphyria
  
MicrobiomeStaphylococcus aureus infections
  
Need for NutrientsApigenin need
 Turmeric (Curcumin)
 Uridine Monophosphate
  
OxidationAntioxidant Capacity
 Oxidative stress
  
Personal characteristicsDouble eyelids
 Eyebrow Thickness
 Straighter hair
 Thicker hair
 Trend to Blond Hair
 Trimethylaminouria (TMAU)
  
Reactions to TreatmentsGlucocorticoid Resistance
 Glucocorticoid Therapy
  
SkinAcne
 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
  
VitaminsVitamin A
 Vitamin B2
 Vitamin B3 (Niacin)
 Vitamin B7 (Biotin)
 Vitamin C
 Vitamin E
  
WeightAdiposity
CategoriesConditions Observed
CancerCervical Neoplasm
 Osteosarcoma
 Tumor Necrosis Factor Alpha
 Tumor calcinosis
  
DentistryBone resorption for prosthesis implants
 Effectiveness in response to bisphosphonates
  
Digestive systemPeroxisomal Enzyme Deficiency
  
Drug ReactionsBetter Response to Methotrexate
  
Genetic diseasesBlau's Syndrome
 Hereditary angioedema
 Hypohydrotic Ectodermal Dysplasia
 Mucolipidosis Type 4 (Gangliosidosis)
 Seckel's Syndrome
 Weaver syndrome
  
Hematologic systemNeuroferritinopathy
  
Hereditary diseasesPompe disease
  
HormoneAcromegaly
 Growth Hormone (GH) Deficiency
  
HormonesEstradiol
 Growth Hormone Response
 Testosterone
  
Immune systemAnkylosing spondylitis
 Lupus
 Lymphedema
 Psoriatic arthritis
  
InflammationsArthrosis of the Knee
 Presence of the HLA-B27 Allele
 Sciatica
 Yao's Syndrome
  
InjuriesFractures
 Hip dislocation
 Meniscus Injury
 Probability of Muscle Injuries
 Read - Repetitive strain injury
 Shoulder Shift
 Sports-Related Musculoskeletal Injuries
  
MetabolicMitochondrial Complex Deficiency 1
  
Metabolic disordersAdenosine Monophosphate Deaminase Deficiency
 Homocystinuria
 Myoadenylate Deaminase Deficiency
  
Muscular systemCalf 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 diseasesMotor Neuropathy
 Peripheral neuropathy
 Progressive Supranuclear Palsy
  
NeurologicalGLUT1 Deficiency Syndrome
  
PainsBack pains
 Lumbar Disc Disease
 Pain Sensitivity
  
PediatricSpina bifida
  
Personal characteristicsAntley-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
  
SportsElbow flexion contracture
 Knee flexion contracture
 Tendon strength
  
Vision (Ophthalmology)Knobloch Syndrome
 Leber's Hereditary Optical Neuropathy (LHON)
 Oculomotor apraxia
CategoriesConditions Observed
AllergiesAllergic 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
  
CancerThyroid Neoplasm
  
CardiovascularProthrombin (G20210A Mutation)
  
Cardiovascular and CerebrovascularPhospholipase Cg2 Defect
  
CellsAutophagy
  
DiabetesEarly 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 systemHirschsprung's Disease (HD)
 Permeable Intestine Syndrome
 Primary Biliary Cirrhosis (CBP)
 Ulcerative Colitis
  
Endocrine systemAutoimmune Thyroid Disease
 Hashimoto's Thyroiditis
 Hashimoto's Thyroiditis (in children)
 Hyperparathyroidism
 Hyperthyroidism
 Hypothyroidism
 Hypothyroidism (Goiter)
 T3
 Thyroid Orbitopathy (OT)
 Thyroid dyshormonogenesis
 Thyrotoxicosis
  
Genetic diseasesFamilial Amyloidotic Polyneuropathy (FAP)
 Family Mediterranean Fever
 Hereditary angioedema
 Hyperimmunoglobulin E (Hyper IgE) Syndrome
 Rasopathies
 Selective IgA Deficiency
  
Hematologic systemActivated 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)
  
HormoneChange of Timo
 Reduction of Thyroid Hormonal Metabolism
 TSH
 Thyroid Function
 
Thyroid Hormone Metabolism (T3: T4 Reduced Ratio)
  
Immune systemAcquired 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)
  
InflammationsBehçet's Disease
 Frontal Fibrosing Alopecia
 Idiopathic inflammatory myopathy
 Inflammatory Bowel Disease (IBD)
 Polymyositis
 Presence of the HLA-B27 Allele
 Sarcoidosis
 Scleroderma
 Sjogren's Syndrome
  
MetabolicCeliac disease
 Gluten Intolerance
 Glycation
 
Greater Insulin Sensitivity with Physical Exercise
 Lactose intolerance
  
Metabolic disordersFetuin-A
  
MethylationMTHFR 1298 mutation (rs1801131)
 MTHFR 677 mutation (rs1801133)
  
Muscular systemMyasthenia Grave
  
Neurodegenerative diseasesCharcot-Marie Disease
 Louis-Bar Syndrome (Ataxia Telangiectasia)
 Multiple sclerosis
 Systemic Sclerosis
  
Respiratory systemChronic obstructive pulmonary disease
  
Skeletal system (bones)Arthritis
 Carpal tunnel syndrome
 Osteoarthritis
 Osteoporosis
 Rheumatoid arthritis
 
Risk of amputation in case of diabetic foot ulcer
  
SkinAlopecia Areata
 Generalized Vitiligo
 Rosacea
 Vitiligo
  
Urinary system
Membranoproliferative Glomerulonephritis (GNMP)
 Nephrotic syndrome
  
Vision (Ophthalmology)Diabetic retinopathy
CategoriesConditions Observed
CancerAcute Lymphoblastic Leukemia (ALL)
 Childhood Acute Lymphoblastic Leukemia
 Childhood Leukemia
 Erythrocytosis
 JAK2 V617F mutation
 Myelodysplastic Syndrome
 Myeloproliferative Disorder
 Peripheral T cell lymphoma
 Polycythemia Vera
  
CardiovascularArginine-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 CerebrovascularHomocysteine Accumulation
 Lipoprotein (a)
  
ClopidogrelResponse to Clopidogrel
  
DiabetesFasting Glucose Level Increase
  
Digestive systemGilbert's Syndrome
  
GeneralALT / AST Index
  
Genetic diseasesA1 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 systemActivated 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 diseasesHereditary Sideroblastic Anemia
  
HormonesHepcidin
  
Immune systemAnti-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)
  
MetabolicCeruloplasmin
 Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency
 Greater Insulin Sensitivity with Physical Exercise
 Lactate dehydrogenase (LDH)
 Methionine Adenosyltransferase Deficiency
  
Metabolic disordersCobalamin Intracellular Metabolism Disease
 Dyslipidemia
 Galactosemia
 Homocystinuria
 Hyperferritinemia
 Low Ferritin
 Myoadenylate Deaminase Deficiency
  
MethylationMTHFR rs1801131
 MTHFR 1298 mutation (rs1801131)
 MTHFR 677 mutation (rs1801133)
 MTHFR rs1801133
  
Need for NutrientsBetaine
 Iron
  
Personal characteristicsToxic Sensitivity to Benzene
  
PharmacogeneticsWarfarin
  
Respiratory systemAspergillosis
 Oxygen Volume (O2) Max (VO2 Max)
  
SkinBasal Blade Disease
 Erythropoietic Protoporphyria
 Hyperchromias
  
Urinary systemGout
 Hematuria
 Uric Acid (Concentration)
  
VitaminsVitamin B3 (Niacin)
CategoriesConditions Observed
Auditory systemNon-syndromic deafness
 Sudden Deafness Syndrome
 Usher Syndrome
  
Breast cancerBreast Neoplasm (Family)
  
CancerBAP1 - 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)
  
CardiovascularBrugada Syndrome
 Familial Hyperlipoproteinemia Type III
 Familial Hypertrophic Cardiomyopathy
 Jervell and Lange-Nielsen Syndrome
 Progressive Familial Heart Block
 Romano-Ward Syndrome
 Sinus Nodule Syndrome
  
DiabetesMODY Type 3 Diabetes
 MODY Type 4 Diabetes
 MODY Type 5 Diabetes
 MODY Type 6 Diabetes
 MODY Type Diabetes
  
Digestive systemAlagille 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
  
GeneralWilliams Syndrome
  
Genetic diseasesAchondroplasia
 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 systemAfibrinogenemia
 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 diseasesFragile X Syndrome
 Friedreich's Ataxia
 Pompe disease
  
Hormones5α-Reductase
 Aromatase Deficiency
  
Immune systemAutoimmune 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)
  
InflammationsSjogren's Syndrome
 Yao's Syndrome
  
MetabolicGlucose-6-Phosphate Dehydrogenase (G6PD) Deficiency
 Mitochondrial Complex Deficiency 1
  
Metabolic disordersAcute Intermittent Porphyria
 Adenosine Monophosphate Deaminase Deficiency
 Cerebrotendinous Xanthomatosis (CTX)
 Fructosemia
 Homocystinuria
 Methylmalonic Acidemia
 Myoadenylate Deaminase Deficiency
 Sanfilippo Syndrome
 Variegate Porphyria
  
Muscular systemBecker 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 diseasesCanavan 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
  
NeurologicalGLUT1 Deficiency Syndrome
 West syndrome
  
Personal characteristicsAntley-Bixley Syndrome with Genital Anomaly
  
PsychiatricRestless Legs Syndrome (Willis-Ekbom disease)
 Tourette's Syndrome
  
Reproductive systemPerrault Syndrome
 Polycystic Ovary Syndrome
  
Skeletal system (bones)Hypochondroplasia
 Léri-Weill dyschondrosteosis
  
SkinEhlers Danlos Syndrome (collagen)
 Erythropoietic Protoporphyria
 Family candidiasis
 KID Syndrome
  
Urinary systemBartter'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 needBiotinidase Deficiency
CategoriesConditions Observed
AllergiesAlcohol Aversion
 Gluten Sensitivity
  
Amino acidsGlutamate Production
 L-theanine
 L-tyrosine
 Serine Deficiency
  
Antioxidants / SupplementsCoenzyme Q10
 Glutathione
 Need for a diet rich in antioxidants
 Probiotics
  
Behavioral ChangesMood Disorder
  
BehaviorsDopamine Levels
  
BenefitChamomile
 S-adenosylmethionine (SAMe)
 Stevia Sweetener Benefit
  
CancerMultiple Endocrine Neoplasm
 Thyroid Neoplasm
  
CardiovascularArginine-succinic aciduria
 Familial Hyperlipoproteinemia Type III
 Hereditary familial hypercholesterolemia
 Hypercholesterolemia (Type B)
  
Cardiovascular and CerebrovascularHomocysteine Accumulation
 Hypertension
 Phospholipase Cg2 Defect
 Sensitivity to Salt (Hypertension)
  
DiabetesCAPN10
 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 systemFamily diarrhea
 Hyperglycinuria
 Hyperlipoproteinemia
 Peroxisomal Enzyme Deficiency
  
Drug ReactionsBetter Response to Methotrexate
  
Endocrine systemAddison'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 AcidsL-lysine
 L-methionine
  
Fatty acidsOmega 6
 Omega 9
  
GeneralAlcohol Intolerance
 Aversion to Vegetables and Coffee
 GS
 INSR
 p70S6K
  
Genetic diseasesAlpha 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 systemAlbumin
 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 diseasesLipotransferase 1 deficiency
  
HormoneAcromegaly
 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)
  
Hormones5α-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 systemAutoimmune Disease
 C3 (immune) deficiency
 Crohn's disease
 Defect in Thyroid Hormonogenesis
 Human Leukocyte Antigen (HLA)
 Mannose Binding Protein Deficiency
  
InflammationsIncreased IL-6 with Vitamin E (Alpha-tocopherol) intake
 Sjogren's Syndrome
  
MetabolicAbility 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 disorders3-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)
  
MitochondriaOxidative Phosphorylation
  
Need for NutrientsApigenin 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 diseasesPeripheral neuropathy
  
OxidationAntioxidant Capacity
 Glutamic Acid Metabolism
 Individuals not expressing CYP3A5
 Oxidative stress
  
Personal characteristicsAlcohol Metabolism
 Greater Stimulus with Caffeine
 
Hypersensitivity to Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)
 Increased Probability of Fatigue
 Mitochondrial Energy Production
 Pineal Hyperplasia
 Spondyloepiphyseal Dysplasia
  
PsychiatricAnorexia Nervosa
  
Reactions to TreatmentsLevothyroxine Combination therapy with Liothyronine
  
Reproductive systemAge at Menarche
 Gestational diabetes
 Polycystic Ovary Syndrome
  
Skeletal system (bones)Development Defects
 Risk of amputation in case of diabetic foot ulcer
  
SkinElastin Deficiency
  
Urinary systemUric Acid (Concentration)
  
Vision (Ophthalmology)Diabetic retinopathy
  
VitaminsFolate
 Vitamin A
 Vitamin B12
 Vitamin B2
 Vitamin B6
 Vitamin B7 (Biotin)
 Vitamin B9 (Folic Acid)
 Vitamin C
 Vitamin D
 Vitamin E
 Vitamin K
  
Vitamins needReduced Conversion of Beta Carotene to Retinol
 Riboflavin Deficiency
  
WeightAbsorption 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
CategoriesConditions Observed
Amino acidsN-acetylcysteine
  
CardiovascularLong 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 StormCCL2 (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
  
GenesIFN-A
 IL-1R
 IL-8
  
Hematologic systemAlpha-Defensins Levels
 Thrombocytopenia
  
Immune systemCCL-3
 CCL-5
 IFN-γ (Interferon-Gamma)
 IFNAR1
 IFNAR2
 IL-12RB1
  
Need for NutrientsLycopene
 Magnesium
 Quercetin
 Selenium
 Zinc
  
Respiratory systemAvian 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
  
VitaminsVitamin A
 Vitamin B1 (Thiamine)
 Vitamin B12
 Vitamin B6
 Vitamin B9 (Folic Acid)
 Vitamin C
 Vitamin D
 Vitamin E
CategoriesConditions Observed
BehavioralCOMT
  
HormonesOxytocin
 Vasopressin (Antidiuretic Hormone - ADH)
  
NeurologicalDopamine Receptors
 Dopamine Synthesis
 Dopamine degradation
 Serotonin Receptors
 Serotonin Synthesis
 Serotonin degradation
CategoriesConditions Observed
GeneralAestuariispira
 Bacteroides_nordii
 Deltaproteobacteria
 EscherichiaShigella
 Klebsiella
 Klebsiella_variicola
 Lactivibrio
 Murimonas
 Paenibacillus
 Pelotomaculum
 Peptoniphilaceae
 Peptoniphilus
  
MicrobiomeAbiotrophy
 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

CategoriesConditions Observed
Need for Nutrients and MetabolismCholine
 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 compositionTendency 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 activityPhysical 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 DeficienciesDeficiency 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 DysfunctionsHypercholesterolemia (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 StressNeed for Detoxification
 Tendency to Oxidative Stress
 IL-10
 IL-1β
 IL-6
 IL-8
 IFN-γ
 TNF
CategoriesConditions Observed
Facial HarmonizationCollagen 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
CategoriesConditions Observed
JointsArthrosis of the Knee
 Osteoarthritis
 Rheumatoid arthritis
 Hip Osteoarthritis
  
Intestinal InflammationsCrohn's disease
 Inflammatory Bowel Disease (IBD)
 Ulcerative Colitis
 Leaky Bowel Syndrome
 Gluten Intolerance
 Lactose intolerance
  
RespiratoryAsthma
 Rhinosinusitis
 Chronic obstructive pulmonary disease
  
Skin InflammationsRosacea
 Atopic Dermatitis
 Contact dermatitis
  
Brain InflammationParkinson's disease
 Alzheimer's disease
 Depression
  
Autoinflammatory DiseasesBlau's Syndrome
 Family Periodic Fever
 Family Mediterranean Fever
 Familial cold autoinflammatory syndrome (FCAS)
 Behcet's Disease
  
C-reactive proteinC-reactive protein
  
Pro-Inflammatory CytokinesIL-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 CytokinesIL-1
 IL-4
 IL-6
 IL-10
 IL-11
 IL-13
 IL-19
 IL-35
 TNF-B
 IFN-A
 IFN-G
 TGF-B
 MIP2
  
ChemokinesCCL2
 CCL3
 CCL5
 CCL7
 CCL8
 CCL11
 CCL13
 CCL17
 CCL19
 CCL22
 CCL25
 CCL27
 CCR1
 CCR2
 CCR3
 CCR5
 CXCR3
 CXCR1
 CCL2
 MIP1A
 MIP1B
 MCP1
  
Hormones and AutoimmuneTestosterone
 Estradiol
 Hypothyroidism
 Cortisol Level
  
OthersRheumatic fever
CategoriesConditions Observed
Allergies and IntolerancesFood 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
  
MethylationMethylation
 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 ProductionMitochondrial Energy Production
 Defect in Carnitine Transport
 Mitochondrial Biogenesis
 Primary Carnitine Deficiency
  
Digestive systemCrohn's disease
 Ulcerative Colitis
 Gastroesophageal Reflux Disease
 Inflammatory Bowel Disease (IBD)
 Celiac disease
  
Antioxidants and DetoxificationOxidative 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)
  
FolateVitamin B9 (Folic Acid)
 Folic Acid Metabolism
 Folate (Vitamin B9)
 MTHFR 1298 mutation (rs1801131)
 
Methylenetetrahydrofolate reductase (MTHFR) deficiency
 Mutation MTHFR 677 (rs1801133)
  
Methionine CycleL-methionine
 Methionine Adenosyltransferase Deficiency
 S-adenosylmethionine (SAMe)
  
Transsulfurization PathwayAmmonia and Glutamate Production
 CBS gene - Transsulfurization
  
NeurotransmittersDopamine 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 CycleGlutathione 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 MineralsVitamin 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
  
ASDAutism (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 / PharmacogeneticsBenefit 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 characteristicsSense 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
  
MicrobiotaClostridium
 Lactobacillus acidophilus
 Probiotics
 Family Candidiasis
 Bifidobacterium
 Lactobacillus
 Clostridium difficile
  
Type of muscle fiberPhysical resistance
 Sprinter
 Endurance
  
Immune systemIgE
 
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 AcidsL-arginine
 L-theanine
 L-lysine
 L-tyrosine
 Serine deficiency
  
Susceptibilities DiseasesAnemia
 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
CategoriesConditions Observed
Other FactorsWaist 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 CellsENPP1
 IRS-1
 GLUT4
 CAPN10
  
Lipid ProfileHDL Cholesterol Level
 Cholesterol Level (LDL)
 Triglycerides
 Dyslipidemia
  
DiabetesType 1 Diabetes
 Type 2 diabetes
 Early Type 2 Diabetes
 Insulin Resistance
 Circulating Glycated Hemoglobin (HbA1c)
 Impairment of β Cell Function
  
Consequences of DiabetesDiabetic neuropathy
 Risk of amputation in case of diabetic foot ulcer
 Diabetic retinopathy
 Increased Risk of Alzheimer's in Diabetics (T2)
 Diabetic heart disease ischemic
  
InsulinHyperinsulinemia
 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
  
PharmacogeneticsResponse to Metformin
 Weight Reduction in Liraglutide Treatment
 GLP-1
 DPP-4
CategoriesConditions Observed
MTHFRMTHFR rs1801131
 MTHFR rs1801133
CategoriesConditions Observed
ProfessionalOpenness 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 ConditionsMorning 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
  
NeurotransmittersDopamine conversion
 Dopamine Synthesis
 Dopamine receptors
 Dopamine degradation
 Dopamine transporters
 Serotonin degradation
 Serotonin receptors
 Serotonin Synthesis
 Serotonin Transporters
  
Behavioral ConditionsPleasantness (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 ConditionsAnorexia Nervosa
 Cataplexy and Narcolepsy (sleep)
 Depression
 Late dyskinesia
 Epilepsy
 Schizophrenia
 Risk of Depression with Parental Divorce
 Suicidal tendencies and thoughts
 Attention Deficit
 Anxiety
  
Psychiatric SyndromesBrunner Syndrome
 Panic Syndrome
 Tourette's Syndrome
  
Personality TraitsPersonality Trait: Extraversion
 Personality Trait: Positive Emotions
 Personality Traits: Hostility, Impulsiveness, Anxiety
 Personality Trait: Assertiveness
 Personality Trait: Conscientiousness
 
Personality Trait: Openness, Altruism, Confidence, and Modesty
  
AdictionsAddition to Heroin
 Addition to Tobacco
 Alcoholism
 Cocaine addiction
 Nicotine Dependence
 Symptoms of Withdrawal in Alcoholism
 Addiction tendency (gambling, alcohol, smoking)
 Alcohol Aversion
  
EmotionalEmotional Insensitivity
 Emotional Insecurity
 Emotional Maturity
 Emotional Negativity
 Emotional Vulnerability
 Relationship Difficulty
  
ConflictsAggressiveness
 Aggression with alcohol consumption
 Antisocial behavior
 Externalizing Behavior
 Self-centeredness
 Indifference
 Neuroticism
 Anger
 Harshness
 Explosive Temperament
 Greater Tendency to Lie
  
DisordersSeasonal 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
CategoriesConditions Observed
NutrientsOmega 3
 Omega 6
  
Hair lossLoss of hair
 Frontal fibrous alopecia
 Congenital Universal Alopecia
 Baldness (Androgenetic Alopecia)
 Alopecia Areata
 Women Baldness
 Male Baldness
 Calvície Feminina
  
Hair FeaturesCurly hair
 Thicker hair
 Straighter hair
 Red hair
 White Hair (Earlier Appearance)
 Pseudofoliculite
  
StructureCollagen Degradation
 Collagen Synthesis
 Ceramides
  
Oxidative StressOxidative stress
 Antioxidant Capacity of the Skin
  
Factors of InfluenceStress
 Anxiety
 Sleep disorder
  
VitaminsVitamin B7 (Biotin)
 Vitamin A
 Vitamin E
 Vitamin B6
 Vitamin C
  
MineralsCopper
 Zinc
 Chrome

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