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)
With Wooly Hair
49 variants Other
X-linked Intellectual Disability-psychosis-macroorchidism Syndrome
49 variants Other
Acetoacetate Levels
48 variants Other
Afap1 Protein Levels
48 variants Other
Ahsg Protein Levels
48 variants Other
And Dysequilibrium Syndrome 1
48 variants Other
Apolipoprotein A1 Levels (ukb Data Field 23440)
48 variants Other
Au-kline Syndrome
48 variants Other
Autosomal Dominant Limb-girdle Muscular Dystrophy Type 1f
48 variants Other
Autosomal Recessive 42
48 variants Other
Autosomal Recessive Bestrophinopathy
48 variants Other
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2m
48 variants Other
Autosomal Recessive Nonsyndromic Hearing Loss 28
48 variants Other
Bardet-biedl Syndrome 15
48 variants Other
Barrett's Esophagus
48 variants Other
Basal Cell Carcinoma (phecode 172.21)
48 variants Cancer
Blmh Protein Levels
48 variants Other
Ccn4 Protein Levels
48 variants Other
Cerebrospinal Fluid Ab1-42 Levels
48 variants Other
Cerebrospinal Fluid T-tau:ab1-42 Ratio
48 variants Other
Charcot-marie-tooth Disease Axonal Type 2f
48 variants Other
Cholesterol Esters in Small Vldl
48 variants Metabolic
Chronic Obstructive Pulmonary Disease X Ever Smoker Interaction (2df)
48 variants Respiratory
Cndp1 Protein Levels
48 variants Other
Cold Induced Vasodilation
48 variants Other
Concentration of Large Vldl Particles (ukb Data Field 23495)
48 variants Other
Congenital Hypothyroidism
48 variants Metabolic
Congenital Myasthenic Syndrome 12
48 variants Other
Coronary Artery Disease or Plasminogen Activator Inhibitor 1 Levels (pleiotropy)
48 variants Cardiovascular
Corpus Callosum Total Area
48 variants Other
Creld1 Protein Levels
48 variants Other
Crigler-najjar Syndrome
48 variants Other
Cstb Protein Levels
48 variants Other
Ctcf-related Neurodevelopmental Disorder
48 variants Other
Cutaneous Melanoma or Hair Colour
48 variants Cancer
Cutaneous Squamous Cell Carcinoma
48 variants Cancer
Deficiency of Hyaluronoglucosaminidase
48 variants Other
Desanto-shinawi Syndrome Due to Wac Point Mutation
48 variants Other
Dilated Cardiomyopathy 1r
48 variants Other
Dorsolateral Prefrontal Area (unadjusted For Global Measures)
48 variants Other
Dpagt1-congenital Disorder of Glycosylation
48 variants Other
Dxa-bone Mineral Density (pelvis) (ukb Data Field 23232)
48 variants Other
Familial Combined Hyperlipidemia Defined By Mexico Criteria
48 variants Metabolic
Fg Syndrome 1
48 variants Other
Flcn-related Disorder
48 variants Other
Flnc-related Disorder
48 variants Other
Frailty (general Factor)
48 variants Other
Free Cholesterol in Medium Hdl (ukb Data Field 23570)
48 variants Metabolic
Gask1a Protein Levels
48 variants Other
Glioma
48 variants Cancer
Glucocorticoid Deficiency with Achalasia
48 variants Other
Glycogen Storage Disease Due to Muscle and Heart Glycogen Synthase Deficiency
48 variants Cardiovascular
Headache
48 variants Other
Hemoglobinopathy
48 variants Hematologic
Hepatocyte Growth Factor Levels
48 variants Other
Hepatocyte Growth Factor-like Protein Levels
48 variants Other
Hypertrophic Cardiomyopathy 10
48 variants Other
Hypertrophic Cardiomyopathy 11
48 variants Other
Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia
48 variants Neurological
Inhbc Protein Levels
48 variants Other
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