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)
Isolated Ectopia Lentis
Isolated Gnrh Deficiency
Isolated Hand Syndactyly
Isolated Noncompaction of the Ventricular Myocardium
Isolated Optic Nerve Hypoplasia
Isopentenyl-diphosphate Delta-isomerase 1 Levels
Isopentenyl-diphosphate Delta-isomerase 2 Levels
Isoursodeoxycholate Levels in Elite Athletes
Isovalerylglycine Levels in Elite Athletes
Ispd-related Disorder
Isx Protein Levels
Itga2-related Disorder
Itga5/itgb7 Protein Level Ratio
Itga5/vcam1 Protein Level Ratio
Itga6-related Disorder
Itgav/itgb5 Protein Level Ratio
Itgb1/itgb2 Protein Level Ratio
Itgb1/mcam Protein Level Ratio
Itgb1/ncam1 Protein Level Ratio
Itgb3-related Disorder
Itgb5/siae Protein Level Ratio
Itih4 Protein Level (protein Group Normalized Intensity)
Itln1 Protein Levels
Itm2b-related Disorder
Itpa-related Disorder
Itpr2-related Disorder
Izumo Sperm-egg Fusion Protein 4 Levels
Jakmip3 Protein Levels
Jam2/thbd Protein Level Ratio
Jam3-related Disorder
Janus Kinase and Microtubule-interacting Protein 3 Levels
Janus Kinase and Microtubule-interacting Protein 3 Levels (jakmip3.9068.17.3)
Jc Polyomavirus Vp1 Antibody Levels
Jiangellaceae Abundance in Stool
Joubert Syndrome 12
Joubert Syndrome 19
Joubert Syndrome 35
Joubert Syndrome 9/15
Joubert Syndrome with Jeune Asphyxiating Thoracic Dystrophy
Junctional Adhesion Molecule B Levels
Junctional Adhesion Molecule-like Levels (amica1.8232.90.3)
Juvenile Recurrent
Juvenile Retinitis Pigmentosa
Kabuki-like Syndrome
Kallikrein
Kallikrein-12 Levels (klk12.3199.54.2)
Kallikrein-14 (analyte X8620.56) Levels
Kallikrein-5 Levels
Kallikrein-6 Levels (klk6.3450.4.2)
Kallikrein-8 Levels (klk8.13708.56.3)
Kank4-related Disorder
Kansl1l Protein Levels
Kaposi Sarcoma
Karayol-borroto-haghshenas Neurodevelopmental Syndrome
Kat6b-related Multiple Congenital Anomalies Syndrome
Kat6b-related Spectrum Disorders
Kazald1/vcam1 Protein Level Ratio
Kcna2-related Disorder
Kcnd2-related Neurodevelopmental Disorder
Kcnd3-related Disorder
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