Health Conditions
43,676 conditions with known genetic associations in our database.
All(43,676)
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)
Metatropic Dysplasia
Mitochondrial Complex 2 Deficiency
Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2
Neurodevelopmental Disorder with or Without Anomalies of the Brain
Number of Decayed, Missing and Filled Tooth Surfaces or Use of Dentures
Ostertag Type
Parsopercularis Area (unadjusted For Global Measures)
Phosphatidylcholine and Other Choline Levels
Phosphatidylethanolamine_38:5_[m-h]1- Levels
Polychlorinated Biphenyl Levels
Predisposition to Invasive Fungal Disease Due to Card9 Deficiency
Ptpn11-related Disorder
Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency Type C
Tert-related Disorder
Tibial Pseudarthrosis
Trem2 Protein Levels
Triacylglycerol(53:3)_[m+nh4]1+ Levels
Triglycerides in Small Ldl (ukb Data Field 23550)
Triglycerides in Small Vldl (ukb Data Field 23515)
Type 2b
Type 2ee
Urinary Calculus (phecode 594)
Ververi-brady Syndrome
12 Conditions
Amy2b Protein Levels
And Cholestasis 1
Aoc3 Protein Levels
Autosomal Dominant 52
Bartter Disease Type 2
Batten-turner Congenital Myopathy
Btn3a2 Protein Levels
Cd163 Protein Levels
Cerebral Cavernous Malformation 3
Charcot-marie-tooth Disease Type 4j
Chronic Sinus Infection
Complement C4 Levels
Concentration of Small Vldl Particles (ukb Data Field 23509)
Congenital Generalized Lipodystrophy Type 1
Deep White Matter Hyperintensities
Diacylglycerol_38:3_[m+h-h2o]1+ Levels
Diacylglycerol_38:5_[m+h-h2o]1+ Levels
Dxa-bone Mineral Density (trunk) (ukb Data Field 23241)
Dync1h1-related Disorder
Encephalomyopathic Form with Methylmalonic Aciduria
Ep-cam Levels
F11 Protein Levels
Fabp9 Protein Levels
Fcer2 Protein Levels
Female-restricted
Flnb-related Disorder
Forns Index in High Alcohol Intake
Ganglion Cell Inner Plexiform Layer (gcipl) Thickness
Grn Protein Levels
Hearing Problems
Hemochromatosis Type 2a
Hypertrophic Cardiomyopathy 6
Immunodeficiency-centromeric Instability-facial Anomalies Syndrome 2
Inferior Parietal Area (unadjusted For Global Measures)
Initial Pursuit Acceleration
Klkb1 Protein Levels
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