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)
Fabp5/pdcd5 Protein Level Ratio
Fabp5/pebp1 Protein Level Ratio
Fabp5/ppcdc Protein Level Ratio
Facial Asymmetry
Facial Emotion Recognition (fearful Faces)
Facial Morphology (d332)
Facial Morphology (d527)
Facial Morphology (d99)
Facial Morphology (jaw Protrusion 2)
Facial Morphology (jaw Protrusion 5)
Facial Morphology (jaw Slope 2)
Facial Morphology (lip Thickness 1)
Facial Morphology (lower Lip Thickness 1)
Facial Morphology (nasion Depth 1)
Facial Morphology (nostril Size)
Facial Morphology (philtrum Length)
Facial Morphology (segment 10)
Facial Morphology (segment 13)
Facial Morphology (segment 19)
Facial Morphology (segment 25)
Facial Morphology (segment 26)
Facial Morphology (segment 27)
Facial Morphology (segment 34)
Facial Morphology (segment 36)
Facial Morphology (segment 38)
Facial Morphology (segment 4)
Facial Morphology (segment 49)
Facial Morphology (segment 54)
Facial Morphology (segment 56)
Facial Morphology (segment 57)
Facial Morphology (segment 59)
Facial Morphology (segment 6)
Facial Nerve Disorders [cn7] (phecode 352.2)
Facial Phenotypes (left Palpebral Fissure Length)
Facial Phenotypes (philtrum Height)
Facial Trait (metopion Eminence Depth)
Facial Wrinkles (principal Components Analysis)
Fadd/nck2 Protein Level Ratio
Fadd/plpbp Protein Level Ratio
Fagerstrӧm Test For Nicotine Dependence
Falls
Fam111a-related Disorder
Fam171a2 Protein Levels
Fam3b/guca2a Protein Level Ratio
Fam3b/tmprss15 Protein Level Ratio
Familial Atrial Fibrillation
Familial Congenital Nasolacrimal Duct Obstruction
Familial Dilated Cardiomyopathy and Peripheral Neuropathy
Familial Episodic Pain Syndrome with Predominantly Upper Body Involvement
Familial Hemophagocytic Lymphohistiocytosis Type 1
Familial Hyperphosphatemic Tumoral Calcinosis/hyperphosphatemic Hyperostosis Syndrome
Familial Hypertrophic Cardiomyopathy 22
Familial Intrahepatic Cholestasis Type 1
Familial Intrahepatic Cholestasis Type 3
Familial Juvenile Type 3
Familial Renal Hypouricemia
Familial Retinal Arterial Macroaneurysm
Familial Scaphocephaly Syndrome
Familial Thoracic
Fanconi Anemia Complementation Group T
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