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)
Alpha-1-antitrypsin Deficiency
And Ophthalmoparesis
Atypical
Cholesteryl Ester Levels in Hdl
Complementation Group 7
Cytochrome B-positive
Neb-related Disorder
Oculocutaneous Albinism Type 1b
Photoreceptor Cell Layer Thickness Phenotypes (mtag)
Rai1-related Disorder
Trichorhinophalangeal Syndrome
Ush2a-related Disorder
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2c
Charcot-marie-tooth Disease Axonal Type 2c
Deficiency of Galactokinase
Dilated
Dystonic Disorder
Intracranial Aneurysm
Noonan Syndrome 9
Problematic Alcohol Use (mtag)
Senior-loken Syndrome 4
Thrombophilia Due to Protein S Deficiency
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2i
Bardet-biedl Syndrome 4
Cleft Lip with or Without Cleft Palate
Congenital Disorder of Deglycosylation
Cryopyrin Associated Periodic Syndrome
Gut Microbial Network Clusters (cyan (at 3 Months) X Any Breastfeeding (3 Months) Interaction
Hyperammonemia
Jervell and Lange-nielsen Syndrome 1
Megalencephalic Leukoencephalopathy with Subcortical Cysts 1
Osteogenesis Imperfecta Type Iii
Pelizaeus-merzbacher Disease
Sphingomyelin(39:1)_[m+h]1+ Levels
Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency Type A
Allergic Rhinitis
Blepharophimosis
Household Income
Monogenic Hearing Loss
Peroxisome Biogenesis Disorder 3a (zellweger)
Pole-related Disorder
Sbbys Type
Thrombophilia Due to Protein C Deficiency
Vertigo
White Blood Cell Count (basophil)
6-pyruvoyl-tetrahydrobiopterin Synthase Deficiency
Blood Urea Nitrogen (bun, Minimum, Inv-norm Transformed)
Carney Complex
Cblb Type
Dilated Cardiomyopathy 1jj
Familial Cold Autoinflammatory Syndrome 2
Hereditary Antithrombin Deficiency
Hereditary Spastic Paraplegia 49
Leukocyte Adhesion Deficiency 1
Mdga1 Protein Levels
Melnick-fraser Syndrome
Multisite Chronic Pain
Peroxisome Biogenesis Disorder 2b
Primary Congenital
Ventricular Fibrillation
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