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)
Cndp1/egfr Protein Level Ratio
Cngb3-related Retinopathy
Cnn2 Protein Levels
Cnpy4/erbin Protein Level Ratio
Cntnap4 Protein Levels
Coatomer Subunit Epsilon Levels
Cocaine Use Disorder
Cocaine Use Disorder X Change in Residence Interaction
Coch-related Disorder
Cochlin Levels (coch.7227.75.3)
Cockayne Spectrum with or Without Cerebrooculofacioskeletal Syndrome
Cofilin-1 Levels (cfl1.4203.50.2)
Cognitive Domain Scores For Executive Function or Language (pleiotropy)
Cognitive Function (executive Function)
Cognitive Function (global Cognition) X Major Depressive Disorder Interaction (1df)
Coiled-coil Domain-containing Protein 134 Levels
Col18a1/retn Protein Level Ratio
Col4a1 or Col4a2-related Cerebral Small Vessel Disease
Col6a3/cst3 Protein Level Ratio
Col6a3/hspg2 Protein Level Ratio
Cole-carpenter Syndrome 1
Colec12/lair1 Protein Level Ratio
Colec12/ltbr Protein Level Ratio
Colipase Levels (clps.5749.53.3)
Colipase-like Protein 1 Levels
Collagen Alpha-1(i) Chain Levels
Collagen Type Ii Levels
Collagen Type Iv Alpha-3-binding Protein Levels
Collectin-11 Levels (colec11.4430.44.3)
Coloboma of Optic Nerve
Combined Immunodeficiency Due to Gins1 Deficiency
Combined Immunodeficiency with Faciooculoskeletal Anomalies
Combined Oxidative Phosphorylation Defect Type 25
Combined Oxidative Phosphorylation Defect Type 30
Combined Oxidative Phosphorylation Defect Type 9
Combined Oxidative Phosphorylation Deficiency 22
Combined Oxidative Phosphorylation Deficiency 48
Combined Oxidative Phosphorylation Deficiency 57
Comm Domain-containing Protein 7 Levels
Comp/thbs4 Protein Level Ratio
Complement C2 Levels
Complement C3 Levels
Complement C3b Levels
Complement Component 1 Q Subcomponent-binding Protein, Mitochondrial Levels
Complement Factor B Deficiency
Complement Factor H-related Protein 4a Levels
Complex Lethal Osteochondrodysplasia
Concomitant Exotropia
Cone-rod Dystrophy 14
Confectionary Intake
Congenital Generalized Lipodystrophy
Congenital Myasthenic Syndrome 2c
Congenital Myopathy 20
Congenital Myopathy 25
Congenital Nonbullous Ichthyosiform Erythroderma
Congenital Septal Defects
Constipation
Continuous Spike and Waves During Slow Sleep
Conventional Bullous Pemphigoid
Copa-related Disorder
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