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)
Cis-urocanate Levels in Elite Athletes
Clec1b/f11r Protein Level Ratio
Clec1b/vsir Protein Level Ratio
Clec1b/yes1 Protein Level Ratio
Clec4d/pglyrp1 Protein Level Ratio
Cleft Palate and Developmental Delay
Clinodactyly of the 5th Finger
Clip2/dapp1 Protein Level Ratio
Cln3-related Disorder
Cln5-related Disorder
Clpb-related Disorder
Cmp-n-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 1 Levels
Cnot1-related Disorder
Cnot3-related Disorder
Cnot9-associated Neurodevelopmental Disorder
Cnpy4/inpp1 Protein Level Ratio
Cnpy4/mesd Protein Level Ratio
Cnpy4/mpi Protein Level Ratio
Cnpy4/tbc1d23 Protein Level Ratio
Cnst/itgb1bp2 Protein Level Ratio
Cntn1/egfr Protein Level Ratio
Cntn2-related Disorder
Cntn3/fetub Protein Level Ratio
Coasy-related Disorder
Coats Plus Syndrome
Coffee Intake (weighted Gwa)
Col6a3/colec12 Protein Level Ratio
Cold Shock Domain-containing Protein C2 Levels
Cold-induced Sweating Syndrome
Cold-induced Sweating Syndrome 2
Colec12/tgfbr2 Protein Level Ratio
Colec12/tnfrsf1a Protein Level Ratio
Collagen Alpha-1(xv) Chain Levels
Collagen Alpha-2(xi) Chain Levels (col11a2.11278.4.3)
Colq-related Disorder
Combined Immunodeficiency Due to Ctps1 Deficiency
Combined Immunodeficiency Due to Moesin Deficiency
Combined Immunodeficiency Due to Ox40 Deficiency
Combined Oxidative Phosphorylation Deficiency 37
Combined Oxidative Phosphorylation Deficiency 56
Combined Oxidative Phosphorylation Deficiency 59
Complement C1q-like Protein 2 Levels
Complement Component C9 Levels
Complement Factor B Levels (cfb.4129.72.1)
Complement Factor H-related Protein 5 Levels (cfhr5.3666.17.4)
Complex Microphthalmia
Composite Immunoglobulin Trait (igg/igm)
Compulsion Score in Obsessive Compulsive Disorder
Concentration of Apixaban (at 3h)
Cone Monochromatism
Congenital Anomalies of Urinary System (phecode 751.2)
Congenital Atn1 Related Disorder
Congenital Bilateral Aplasia Of
Congenital Bile Acid Synthesis Defect 4
Congenital Communicating
Congenital Contracture
Congenital Disorders of Glycosylation Type Ii
Congenital Hearing Loss
Congenital Titinopathy
Cop9 Signalosome Complex Subunit 7b Levels
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