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)
Hair Colour (natural, Before Greying): Red (ukb Data Field 1747_2)
Hearing Difficulty
Immature Platelet Count
Joubert Syndrome with Renal Defect
Juvenile Retinoschisis
Kidney Sinus Volume
Kleefstra Syndrome 2
Mitochondrial Dna Copy Number (adjusted)
Neonatal Form
Phospholipid Levels in Hdl
Phospholipid Levels in Small Vldl
Sick Sinus Syndrome 1
Subcortical Volume (min-p)
Sulfite Oxidase Deficiency
Symmetrical Dyschromatosis of Extremities
Syndromic X-linked Intellectual Disability Najm Type
Total Lipid Levels in Large Vldl
Total Lipid Levels in Small Vldl
6-month Creatinine Clearance Change Response to Tenofovir Treatment in Hiv Infection (treatment Arm Interaction)
Anophthalmia-microphthalmia Syndrome
Ascending Aorta Maximum Area
Autosomal Recessive Ataxia Due to Ubiquinone Deficiency
Coronary Artery Disease or Von Willebrand Factor Levels (pleiotropy)
Fbn1-related Disorder
Femoral Neck Bone Mineral Density
Hematocrit (minimum, Inv-norm Transformed)
Inflammatory Bowel Disease (tractor Method with European Ancestry)
Inflammatory Skin Disease
Keratinocyte Cancer (mtag)
Nonalcoholic Fatty Liver Disease (imputed)
Papillon-lefèvre Syndrome
Phosphatidylcholine(38:3)_[m+h]1+/phosphatidylethanolamine(41:3)_[m+h]1+/phosphatidate(43:4)_[m+nh4]1+ Levels
Phospholipid Levels in Medium Hdl
Piezo1-related Disorder
Progressive Familial Intrahepatic Cholestasis Type 3
Response to Amphetamines
Retinal Arteriolar Tortuosity
Somatic
Trail Levels
Triglyceride Levels in Small Hdl
1,5-anhydroglucitol (1,5-ag) Levels
3m Syndrome 2
Alg9 Congenital Disorder of Glycosylation
Aneurysm-osteoarthritis Syndrome
Bilirubin Levels
Cholesterol to Total Lipids Ratio in Very Large Vldl
Coffin-lowry Syndrome
Complement Component 3 Deficiency
Congenital Microvillous Atrophy
Cpvl Protein Levels
Developmental and Epileptic Encephalopathy 6b
Elevated Prostate Specific Antigen [psa] (phecode 796)
Family History of Alzheimer's Disease
Free Cholesterol to Total Lipids Ratio in Very Small Vldl
Gracile Syndrome
Hereditary Mixed
Hypercalcemia
Inflammatory Bowel Disease 1
Leber Congenital Amaurosis 4
Major Depressive Disorder (mtag)
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