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)
Combined Immunodeficiency Due to Ctps1 Deficiency
4 variants Other
Combined Immunodeficiency Due to Moesin Deficiency
4 variants Other
Combined Immunodeficiency Due to Ox40 Deficiency
4 variants Other
Combined Oxidative Phosphorylation Deficiency 37
4 variants Other
Combined Oxidative Phosphorylation Deficiency 56
4 variants Other
Combined Oxidative Phosphorylation Deficiency 59
4 variants Other
Comorbidity of Gastric and Duodenal Ulcers
4 variants Gastrointestinal
Complement C1q Tumor Necrosis Factor-related Protein 1 Levels (c1qtnf1.6304.8.3)
4 variants Cancer
Complement C1q-like Protein 2 Levels
4 variants Other
Complement Component C9 Levels
4 variants Other
Complement Factor B Levels (cfb.4129.72.1)
4 variants Other
Complement Factor H-related Protein 5 Levels (cfhr5.3666.17.4)
4 variants Other
Complex Microphthalmia
4 variants Other
Composite Immunoglobulin Trait (igg/igm)
4 variants Other
Compulsion Score in Obsessive Compulsive Disorder
4 variants Other
Concentration of Apixaban (at 3h)
4 variants Other
Cone Monochromatism
4 variants Other
Congenital Anomalies of Urinary System (phecode 751.2)
4 variants Other
Congenital Atn1 Related Disorder
4 variants Other
Congenital Bilateral Aplasia Of
4 variants Other
Congenital Bile Acid Synthesis Defect 4
4 variants Other
Congenital Communicating
4 variants Other
Congenital Contracture
4 variants Other
Congenital Disorders of Glycosylation Type Ii
4 variants Other
Congenital Hearing Loss
4 variants Other
Congenital Myopathy 21 with Early Respiratory Failure
4 variants Respiratory
Congenital Titinopathy
4 variants Other
Cop9 Signalosome Complex Subunit 7b Levels
4 variants Other
Coq2-related Disorder
4 variants Other
Coq6-related Disorder
4 variants Other
Coq8b-related Disorder
4 variants Other
Corneal Intraepithelial Dyskeratosis-palmoplantar Hyperkeratosis-laryngeal Dyskeratosis Syndrome
4 variants Other
Corticosteroid-binding Globulin Deficiency
4 variants Other
Cortisol Levels
4 variants Other
Cortisone Levels
4 variants Other
Cortisone Levels in Elite Athletes
4 variants Other
Cortolone Glucuronide (1) (x-17359) Levels
4 variants Other
Covid-19 (critical Illness Vs Mild Symptoms)
4 variants Other
Covid-19 (severe Vs Population) X Sex Interaction
4 variants Other
Covid-19 Infection or Bmi (pleiotropy)
4 variants Metabolic
Cox5b/metap1d Protein Level Ratio
4 variants Other
Cpb1/ctrc Protein Level Ratio
4 variants Other
Cpxm1/mdk Protein Level Ratio
4 variants Other
Cpxm1/sparc Protein Level Ratio
4 variants Other
Cpxm1/vegfc Protein Level Ratio
4 variants Other
Cradd/dars1 Protein Level Ratio
4 variants Other
Cradd/sirt2 Protein Level Ratio
4 variants Other
Cradd/tbcb Protein Level Ratio
4 variants Other
Cranial Vault Shape (segment 11)
4 variants Other
Cranial Vault Shape (segment 5)
4 variants Other
Craniofacial Microsomia 2
4 variants Other
Craniosynostosis 2
4 variants Other
Craniosynostosis with Ectopia Lentis
4 variants Other
Crb1-related Maculopathy
4 variants Other
Creatine Kinase Levels in Statin Users
4 variants Pharmacogenomic
Creatine Kinase M-type:creatine Kinase B-type Heterodimer Levels
4 variants Other
Creg1/pla2g15 Protein Level Ratio
4 variants Other
Creld2/sumf2 Protein Level Ratio
4 variants Other
Creld2/txndc5 Protein Level Ratio
4 variants Other
Crkl/egf Protein Level Ratio
4 variants Other
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