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)
Menke-hennekam Syndrome 1
Perrault Syndrome 1
Phenylalanine Levels
Phosphatidylinositol(38:4)_[m-h]1- Levels
Pneumonia
Progressive
Prostate-specific Antigen (psa, Maximum, Inv-norm Transformed)
Pyknodysostosis
Short Qt Syndrome Type 3
Sitosterolemia
Spinocerebellar Ataxia Type 6
Twist1-related Craniosynostosis
Velocity At Peak Velocity
Albumin (mean, Inv-norm Transformed)
Bardet-biedl Syndrome 20
Deficiency of Steroid 17-alpha-monooxygenase
Hemolytic Uremic Syndrome
Hereditary Spherocytosis Type 2
Juvenile
Lissencephaly Due to Tuba1a Mutation
Paroxysmal Familial
Pnliprp2 Protein Levels
Postaxial
Sodium (mean, Inv-norm Transformed)
Tnfrsf10c Protein Levels
Treh Protein Levels
Verbal-numerical Reasoning
Abnormal Bleeding
Body Fat Distribution (leg Fat Ratio)
Body Mass Index in Physically Active Individuals
Combined Immunodeficiency Due to Partial Rag1 Deficiency
Congenital Myasthenic Syndrome 4c
Fatty Acid(20:4)_[m-h]1- Levels
Hermansky-pudlak Syndrome 2
Holt-oram Syndrome
Hyper-ige Recurrent Infection Syndrome 1
Icam4 Protein Levels
Ichthyosis Vulgaris
Leisure Screen Time
Lymphocyte (absolute Count, Minimum, Inv-norm Transformed)
Mendelian Susceptibility to Mycobacterial Diseases Due to Complete Il12rb1 Deficiency
Omega-6 Fatty Acids to Omega-3 Fatty Acids Ratio
Pontoneocerebellar Hypoplasia
Pre-treatment Viral Load in Hiv-1 Infection
Short-rib Thoracic Dysplasia 7 with or Without Polydactyly
Spatial Qrs-t Angle
Triglyceride Levels in Small Ldl
3-oxo-5 Alpha-steroid Delta 4-dehydrogenase Deficiency
Cholesteryl Ester Levels in Medium Hdl
Cholesteryl Esters in Large Vldl
Deficiency of Hydroxymethylglutaryl-coa Lyase
Dubin-johnson Syndrome
Hair Colour (natural, Before Greying): Red (ukb Data Field 1747_2)
Hearing Difficulty
Juvenile Retinoschisis
Kleefstra Syndrome 2
Mitochondrial Dna Copy Number (adjusted)
Neonatal Form
Sick Sinus Syndrome 1
Subcortical Volume (min-p)
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