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)
Ccl3 Levels
12 variants Other
Ccn5 Protein Levels
12 variants Other
Cd7 Protein Levels
12 variants Other
Cdc42bpb-related Neurodevelopmental Syndrome
12 variants Other
Cdkn1a/tacc3 Protein Level Ratio
12 variants Other
Cenpf-related Disorder
12 variants Other
Cenpj-related Disorder
12 variants Other
Ceramide (d19:1/18:0) Levels
12 variants Other
Ceramide (d20:1/22:0) Levels
12 variants Other
Ceramide Levels (c24:0)
12 variants Other
Cerebral Aneurysm
12 variants Other
Cerebrospinal Fluid P-tau Levels
12 variants Other
Chad Protein Levels
12 variants Other
Charcot-marie-tooth Disease Axonal Type 2l
12 variants Other
Charcot-marie-tooth Disease Type 2b
12 variants Other
Chd2-related Disorder
12 variants Other
Chordoma
12 variants Other
Chylomicron Retention Disease
12 variants Other
Circulating Leptin Levels or Type 2 Diabetes
12 variants Metabolic
Cis-4-decenoylcarnitine (c10:1) Levels in Elite Athletes
12 variants Other
Classic Dopamine Transporter Deficiency Syndrome
12 variants Other
Clcn4-related Disorder
12 variants Other
Clozapine-induced Agranulocytosis/granulocytopenia in Treatment-resistant Schizophrenia
12 variants Neurological
Col17a1-related Disorder
12 variants Other
Col6a3 Protein Levels
12 variants Other
Col9a1 Protein Levels
12 variants Other
Combined Osteogenesis Imperfecta and Ehlers-danlos Syndrome 1
12 variants Other
Common Carotid Intima-media Thickness in Hiv Infection
12 variants Other
Conduct Disorder
12 variants Other
Cone-rod Dystrophy 11
12 variants Other
Congenital Anomalies of the Integument (phecode 757)
12 variants Other
Congenital Myasthenic Syndrome 14
12 variants Other
Congenital Neutropenia-myelofibrosis-nephromegaly Syndrome
12 variants Renal
Congenital Nongoitrous Hypothyroidism 6
12 variants Metabolic
Congestive Heart Failure; Nonhypertensive (phecode 428)
12 variants Cardiovascular
Contactin-4 Levels
12 variants Other
Copper Levels
12 variants Other
Coq8a-related Disorder
12 variants Other
Corneal Dystrophy (phecode 364.5)
12 variants Other
Coronary Artery Calcification in Type 2 Diabetes (excluding Prevalent Cardiovascular Disease)
12 variants Cardiovascular
Cpn1 Protein Levels
12 variants Other
Cpn2 Protein Levels
12 variants Other
Craniofacial-deafness-hand Syndrome
12 variants Other
Ctnnb1-related Disorder
12 variants Other
Cul7-related Disorder
12 variants Other
Cxadr Protein Levels
12 variants Other
Cxcl13 Protein Levels
12 variants Other
Cxcl17 Protein Levels
12 variants Other
Cystatin C Levels X Vegetarianism Interaction
12 variants Pharmacogenomic
Dandy-walker Syndrome
12 variants Other
Dbi/edar Protein Level Ratio
12 variants Other
Dbnl/edar Protein Level Ratio
12 variants Other
Ddah1 Protein Levels
12 variants Other
Declining Hemoglobin Trajectory in Blood Donors
12 variants Hematologic
Deficiency of Ribose-5-phosphate Isomerase
12 variants Other
Delayed Gross Motor Development
12 variants Other
Depressive Symptoms X Dependent Stressful Life Events Interaction (1df Test)
12 variants Other
Developmental and Epileptic Encephalopathy 89
12 variants Other
Developmental Dysplasia of the Hip
12 variants Other
Diamond-blackfan Anemia 5
12 variants Hematologic
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