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)
Ceramide (d16:1/18:0) Levels
Ceramide (d16:1/22:0) Levels
Ceramide (d17:1/24:1) Levels
Ceramide (d18:1/20:0) Levels
Ceramide (d18:2/24:1, D18:1/24:2) Levels in Elite Athletes
Ceramide (d19:1/26:0) Levels
Cerebellum White Matter Volume
Cerebellum White Matter Volume Change Rate X Age Interaction (1df)
Cerebral Aneurysm (phecode 433.5)
Cerebral White Matter Volume Change Rate X Age Interaction (2df)
Change in High-sensitivity Cardiac Troponin I Concentration
Char Syndrome
Charcot-marie-tooth Disease Axonal Type 2cc
Chediak-higashi Syndrome
Chilton-okur-chung Neurodevelopmental Syndrome
Choanal Atresia-hearing Loss-cardiac Defects-craniofacial Dysmorphism Syndrome
Cholesteryl Ester (24:5) Levels
Chrna4-related Disorder
Chronic Bronchitis and Chronic Obstructive Pulmonary Disease
Chronic Central Serous Retinopathy
Chronic Heart Failure
Chronic Obstructive Pulmonary Disease (moderate to Severe)
Chronic Obstructive Pulmonary Disease or Irritable Bowel Syndrome (mtag)
Chronic Rhinosinusitis (mtag)
Chronic Ulcer of Skin (phecode 707)
Chronotype and Er- Breast Cancer
Clcn7-related Disorder
Clec3b Protein Levels
Cleft Lip with or Without Cleft Palate X Maternal Periconceptional Smoking Interaction (parent of Origin Effect)
Cleft Palate with Ankyloglossia
Cmc1 Protein Levels
Coagulation Factor X Levels
Coagulation Factor Xa Levels
Coffee Type: Decaffeinated Coffee (any Type) (ukb Data Field 1508_1)
Cohen-gibson Syndrome
Col15a1 Protein Levels
Colonic Neoplasm
Colorectal Cancer Vs Inflammatory Bowel Disease or Controls
Colorectal Cancer X Cheese Intake Interaction
Combined Partial
Complex Regional/central Pain Syndrome (phecode 355)
Composite Immunoglobulin Trait (iga/igm)
Comprehensive Assessment of Prospective Memory Instrumental Activities of Daily Living (capm Iadl)
Comt/itgb1bp2 Protein Level Ratio
Congenital Absence of Salivary Gland
Congenital Anomalies of Skin (phecode 691)
Congenital Brain Dysgenesis Due to Glutamine Synthetase Deficiency
Congenital Malabsorptive Diarrhea 4
Congenital Muscular Dystrophy with Intellectual Disability and Severe Epilepsy
Congenital Myopathy 10b
Congenital Myopathy 2b
Congenital Sensorineural Hearing Impairment
Congenital Stationary Night Blindness Autosomal Dominant 3
Congenital Symmetric Circumferential
Conjugated Linoleic Acid
Contactin-1 Levels
Cooked Vegetable Consumption
Coprococcus Comes
Coq7 Protein Levels
Corneal Opacity and Other Disorders of Cornea (phecode 364)
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