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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