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)
Collagen Alpha-1(vi) Chain Levels
Collagen Alpha-1(x) Chain Levels
Collagen Alpha-1(xiii) Chain Levels
Collagen Alpha-2(ix) Chain Levels (col9a2.9804.11.3)
Collagen Alpha-2(xi) Chain Levels
Collagen Alpha-3(vi) Chain Levels
Collagen Triple Helix Repeat-containing Protein 1 Levels
Collagen Type Iii Levels
Collagenase 3 Levels
Collectin-10 Levels (colec10.6558.5.3)
Collectin-12 (analyte X5457.5) Levels
Collectin-12 Levels (colec12.5457.5.2)
Colonic Diverticula
Combined or Isolated
Combined Oxidative Phosphorylation Deficiency 41
Combined Oxidative Phosphorylation Deficiency 43
Comm Domain-containing Protein 9 Levels
Commd9 Protein Levels
Complement C1r Subcomponent-like Protein Levels (c1rl.9348.1.3)
Complement Component 4b Deficiency
Complement Component C7 (analyte X2888.49) Levels
Complement Decay-accelerating Factor Levels (cd55.5069.9.3)
Complement Factor H Levels (cfh.4159.130.1)
Complement Factor H-related Protein 5 (analyte X7885.17) Levels
Complex Febrile Seizure
Composite Immunoglobulin Trait (iga X Igg X Igm)
Comprehensive Listening
Comprehensive Strength and Appendicular Lean Mass
Comt/rhoc Protein Level Ratio
Concentration of Apixaban (at 9h)
Concentric Hypertrophic Cardiomyopathy
Concussion
Concussion (phecode 817)
Conductive Hearing Impairment
Cone-rod Dystrophy 22
Cone-rod Dystrophy 23
Congenital Bilateral Absence of Vas Deferens
Congenital Bile Acid Synthesis Defect
Congenital Disorder of Glycosylation Type I
Congenital Generalized
Congenital Myopathy 15
Congenital Nystagmus
Congenital Plasminogen Activator Inhibitor Type 1 Deficiency
Congenital Proximal
Congenital Scoliosis
Congenital Structural Myopathy
Conjunctivitis, Noninfectious (phecode 371.2)
Connatal
Connective Tissue Dysplasia
Conotruncal Anomaly Face Syndrome
Conscientiousness
Contactin-2 Levels (cntn2.3296.92.2)
Contactin-4 Levels (cntn4.3298.52.2)
Contactin-5 Levels (cntn5.3299.29.2)
Contamination Dimension in Obsessive Compulsive Disorder
Cop9 Signalosome Complex Subunit 2 Levels
Cop9 Signalosome Complex Subunit 2 Levels (cops2.14029.42.3)
Copa Protein Levels
Copper Chaperone For Superoxide Dismutase Levels
Copper Transport Protein Atox1 Levels
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