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)
Alanine Levels
Eosinophil (fraction, Maximum, Inv-norm Transformed)
Gm1 Gangliosidosis
Concentration of Chylomicrons and Extremely Large Vldl Particles
Free Cholesterol in Very Large Hdl
Saguenay-lac-saint-jean Type
Aortic Valve Disease 1
Cognitive Ability, Years of Educational Attainment or Schizophrenia (pleiotropy)
Deafness
Epidermolysis Bullosa
Hip Circumference (ukb Data Field 49)
Mismatch Repair Cancer Syndrome 1
Severe Neonatal-onset Encephalopathy with Microcephaly
Short Stature
Aspartate Aminotransferase Levels (ukb Data Field 30650)
Charcot-marie-tooth Disease Axonal Type 2v
Long Chain 3-hydroxyacyl-coa Dehydrogenase Deficiency
Multiple Endocrine Neoplasia Type 2a
Alpha Thalassemia-x-linked Intellectual Disability Syndrome
Body Mass Index (bmi, Mean, Inv-normal Transformed)
Central Corneal Thickness (mtag)
Cholestasis
Severe X-linked Myotubular Myopathy
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
Autosomal Recessive Distal Spinal Muscular Atrophy 1
Concentration of Very Large Vldl Particles
Autosomal Dominant 4
Autosomal Recessive Nonsyndromic Hearing Loss 77
Concentration of Large Vldl Particles
Non-melanoma Skin Cancer
Ornithine Carbamoyltransferase Deficiency
Well-being Spectrum (multivariate Analysis)
Autosomal Dominant Nonsyndromic Hearing Loss 6
Body Mass Index (bmi, Maximum, Inv-normal Transformed)
Gne Myopathy
Leber Congenital Amaurosis 2
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions
Red Cell Diameter Width (rdw, Mean, Inv-norm Transformed)
Tooth Agenesis
Total Protein Levels (ukb Data Field 30860)
Blood Cell Traits Latent Factor 9 (white Cell)
Cbs-related
Fanconi Anemia Complementation Group N
Free Cholesterol Levels in Chylomicrons and Extremely Large Vldl
Hyperhomocysteinemia
Thrombotic
Cholesterol to Total Lipids in Large Hdl Percentage
Prph2-related Disorder
Alcohol Consumption (drinks Per Week) (mtag)
Argininosuccinate Lyase Deficiency
Concentration of Small Vldl Particles
High Density Lipoprotein Cholesterol (hdlc, Mean, Inv-norm Transformed)
Charcot-marie-tooth Disease Axonal Type 2s
Common Executive Function
Direct Bilirubin Levels
Facial Appearance
Hdl Cholesterol Levels (ukb Data Field 30760)
Hemoglobin A1c (hba1c, Mean, Inv-norm Transformed)
Pkhd1-related Disorder
Autosomal Recessive Congenital Ichthyosis 1
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →