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)
Familial Cylindromatosis
Free Cholesterol in Ldl (ukb Data Field 23421)
Gamma-glutamyl-alpha-lysine Levels
Gaucher Disease-ophthalmoplegia-cardiovascular Calcification Syndrome
Gut Microbiome Abundance (class Bacteroides Thetaiotaomicron (at 3 Months) X Household Furry Pet Cat (3 Months) Interaction
Gys1 Protein Levels
Gzmb Protein Levels
Hdl X Anxiety Interaction (2df Test)
Hereditary Cryohydrocytosis with Reduced Stomatin
Hereditary Motor and Sensory Neuropathy with Optic Atrophy
Hypermetropia (phecode 367.8)
Hyperuricemia in High Vitamin E Intake
Hyperuricemia in Low Fat Intake
Hyperuricemia in Low Protein Intake
Immature Reticulocyte Forward Scatter
Inborn Error of Immunity
Information Processing Speed
Intestinal Gastric Cancer
Klk15 Protein Levels
Kynurenate Levels
Kynurenine Levels
Leber Congenital Amaurosis 11
Left Ventricle Wall Thickness
Lethal
Leukoencephalopathy with Vanishing White Matter 5
Low Phospholipid Associated Cholelithiasis
Lpo Protein Levels
Major Depressive Episode Treated with Electroconvulsive Therapy
Mandibuloacral Dysplasia with Type A Lipodystrophy
Mansc1 Protein Levels
Marco Protein Levels
Masa Syndrome
Mean Bone Marrow Fat Fraction of Lumbar Vertebrae 1-5
Methyl Glucopyranoside (alpha + Beta) Levels
Microcephaly 7
Microphthalmia with Brain and Digit Anomalies
Mrc1 Protein Levels
Nephronophthisis 9
Neurodevelopmental Disorder with Cerebellar Atrophy and with or Without Seizures
Neurodevelopmental Disorder with Language Impairment and Behavioral Abnormalities
Nonsyndromic Oculocutaneous Albinism
Npy Protein Levels
Occupational Attainment
Occupational Creativity
Osteonecrosis (time to Event) in Systemic Lupus Erythematosus
Partial
Pdgfa Protein Levels
Peroxisome Biogenesis Disorder 2a (zellweger)
Pex6-related Disorder
Pharc Syndrome
Phosphatidylethanolamine (18:0_20:4) Levels
Phosphatidylethanolamine_36:2_[m-h]1- Levels
Phospholipids to Total Lipids in Very Large Vldl Percentage (ukb Data Field 23584)
Platelet Aggregation
Polyhydramnios
Primary Ciliary Dyskinesia 11
Progression Free Survival in Epithelial Ovarian Cancer Treated with Carboplatin and Paclitaxel
Quinolinate Levels
Rarres1 Protein Levels
Renal Tubulopathies
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