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)
Breast Cancer in Brca1 Mutation Carriers
Broad Depression or Schizophrenia
C-c Motif Chemokine 3 Levels
C-x-c Motif Chemokine 11 Levels
Ca3 Protein Levels
Ca9 Protein Levels
Cafe Au Lait Spots
Calcium Levels X Vegetarianism Interaction
Carasil Syndrome
Carbohydrate Antigen 19-9 Levels
Cardiac Valvular Defect
Cardiac Valvular Type
Cataract 21 Multiple Types
Ccdc88c-related Disorder
Ccl19 Protein Levels
Ccl7 Protein Levels
Cd109 Antigen Levels
Cd4 Protein Levels
Cdkn2d/itgb1bp2 Protein Level Ratio
Ceacam1 Protein Levels
Central Cerebrospinal Fluid Amyloid Beta 42 to 40 Ratio
Central Hypoventilation Syndrome
Cep164-related Disorder
Ceramide (d19:1/20:0) Levels
Ceramide(41:0)_[m-h]1- Levels
Cerebellar Ataxia-hypogonadism Syndrome
Cerebellar Vermis Hypoplasia
Cerebellum Cortex Volume
Cerebral Amyloid Angiopathy in Alzheimer’s Disease
Cerebral Calcification
Cerebrospinal Ab1-42 Levels in Normal Cognition
Cervical High-risk Human Papilloma Virus Infection (persistent)
Childhood Wheezing (pre-school Remitting)
Chime Syndrome
Cholesterol
Cholesteryl Esters in Very Large Hdl
Cholesteryl Esters to Total Lipids in Chylomicrons and Extremely Large Vldl Percentage (ukb Data Field 23581)
Choline Levels
Chrne-related Disorder
Cigarette Consumption X Playing Computer Games Interaction
Circulating Leptin Levels
Cirrhosis (alcohol Related)
Clc Protein Levels
Clec14a Protein Levels
Clozapine-induced Cytotoxicity
Cnga3-related Disorder
Coagulation Factor Xi Levels
Cognitive Function (kinship Model)
Cognitive Function (processing Speed) X Major Depressive Disorder Interaction (1df)
Cognitive Performance (global Cognitive Function) (longitudinal)
Col9a1-related Disorder
Combined Oxidative Phosphorylation Defect Type 15
Combined Oxidative Phosphorylation Deficiency 55
Common Traits (other)
Complement Component 5 Deficiency
Complex Cortical Dysplasia with Other Brain Malformations 6
Congenital Anomalies of Face and Neck (phecode 749)
Congenital Sensory Neuropathy with Selective Loss of Small Myelinated Fibers
Congenital Stationary Night Blindness 1b
Congenital Stationary Night Blindness 1f
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