Health Conditions

52,757 conditions with known genetic associations in our database.

All(52,757) Other(43,676) Cardiovascular(1,793) Metabolic(1,614) Renal(1,319) Cancer(1,257) Neurological(750) Ophthalmic(535) Gastrointestinal(367) Hematologic(345) Respiratory(323) Autoimmune(265) Dermatologic(221) Pharmacogenomic(163) Musculoskeletal(129)
Anticoagulants Causing Adverse Effects (phecode 964.1)
11 variants Other
Antipsychotic-induced Triglycerides Change in Schizophrenia (6-week)
11 variants Neurological
Anxiety and Stress-related Disorders
11 variants Other
Ap5z1-related Disorder
11 variants Other
Apolipoprotein E Levels
11 variants Other
App/pdgfb Protein Level Ratio
11 variants Other
Arg1/hmbs Protein Level Ratio
11 variants Other
Arhgap31-related Disorder
11 variants Other
Arhgef12/axin1 Protein Level Ratio
11 variants Other
Arm Fat Ratio or Colorectal Cancer (pleiotropy)
11 variants Cancer
Arrhythmogenic Right Ventricular Dysplasia
11 variants Other
Asgr1 Protein Levels
11 variants Other
Aspartate Aminotransferase Levels X Vegetarianism Interaction
11 variants Other
Asthma in Gastrointestinal Disease
11 variants Respiratory
Atherosclerosis (phecode 440)
11 variants Cardiovascular
Atox1 Protein Levels
11 variants Other
Atp1a2-related Disorder
11 variants Other
Atrial Conduction Disease
11 variants Other
Attention Deficit Hyperactivity Disorder (time to Onset)
11 variants Other
Autoimmune Hepatitis Type-1
11 variants Autoimmune
Autosomal Dominant 66
11 variants Other
Autosomal Dominant Limb-girdle Muscular Dystrophy Type 1g
11 variants Other
Autosomal Dominant Nonsyndromic Hearing Loss 25
11 variants Other
Autosomal Dominant Parkinson Disease 1
11 variants Neurological
Autosomal Recessive 26
11 variants Other
Autosomal Recessive 58
11 variants Other
Autosomal Recessive 77
11 variants Other
Autosomal Recessive Kenny-caffey Syndrome
11 variants Other
Autosomal Recessive Mendelian Susceptibility to Mycobacterial Diseases Due to Complete Rorgamma Receptor Deficiency
11 variants Other
Autosomal Recessive Nonsyndromic Hearing Loss 32
11 variants Other
Auts2-related Disorder
11 variants Other
Axin1/itgb1bp2 Protein Level Ratio
11 variants Other
Axin2-related Attenuated Familial Adenomatous Polyposis
11 variants Other
B2m Protein Levels
11 variants Other
Bach1/hexim1 Protein Level Ratio
11 variants Other
Bain Type
11 variants Other
Bckdha-related Disorder
11 variants Other
Bcr/itgb1bp2 Protein Level Ratio
11 variants Other
Beta Thalassemia Intermedia
11 variants Hematologic
Bioavailable Testosterone Levels X Vegetarianism Interaction
11 variants Other
Biological Age (phenoage)
11 variants Other
Biological Mother: High Cholesterol
11 variants Metabolic
Biotin-responsive
11 variants Other
Blood Trace Element (zn Levels)
11 variants Other
Bmi X Environmental Factors (excluding Physical Activity) Interaction
11 variants Metabolic
Bmp4 Protein Levels
11 variants Other
Body Fat Percentage and Type 2 Diabetes (pairwise)
11 variants Metabolic
Body Mass Index (age <50)
11 variants Other
Body Mass Index and Systole Blood Pressure (pairwise)
11 variants Cardiovascular
Bone Mineral Density (paediatric, Skull)
11 variants Other
Bone Properties (heel)
11 variants Other
Braf-related Disorder
11 variants Other
Brain Connectivity
11 variants Other
Brain Imaging Abnormality
11 variants Other
Brca1 Mutation in Breast Cancer
11 variants Cancer
Brugada Syndrome 9
11 variants Other
Bryant-li-bhoj Neurodevelopmental Syndrome 2
11 variants Other
C-c Motif Chemokine 23 Levels
11 variants Other
C1q Deficiency
11 variants Other
Caffeine Metabolism (plasma 1,3,7-trimethylxanthine (caffeine) Level)
11 variants Pharmacogenomic
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