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)
Autosomal Recessive 110
Autosomal Recessive 14
Autosomal Recessive 34
Autosomal Recessive 46
Autosomal Recessive 71
Autosomal Recessive Congenital Ichthyosis 11
Autosomal Recessive Congenital Ichthyosis 9
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2w
Autosomal Recessive Nonsyndromic Hearing Loss 102
Autosomal Recessive Nonsyndromic Hearing Loss 61
Autosomal Recessive Nonsyndromic Hearing Loss 93
Autosomal Recessive Omodysplasia
Autosomal Recessive Optic Atrophy
Autosomal Recessive Spinocerebellar Ataxia 15
Autosomal Recessive Spinocerebellar Ataxia 18
Axin-2 Levels (axin2.8429.16.3)
Axin1/ikbkg Protein Level Ratio
Axin1/irak4 Protein Level Ratio
Axl/il18bp Protein Level Ratio
B3glct-related Disorder
Bach1/nfatc1 Protein Level Ratio
Bag3 Protein Levels
Bank1 Protein Levels
Bank1/sh2b3 Protein Level Ratio
Bannayan-riley-ruvalcaba Syndrome
Bardet-biedl Syndrome 19
Bartter Syndrome with Hypocalcemia
Baz2b-related Disorder
Bcan/mog Protein Level Ratio
Bche-related Disorder
Bcl11b-related Disorder
Bcl2l15 Protein Levels
Bcr/nfatc1 Protein Level Ratio
Bcr/plxna4 Protein Level Ratio
Bernard-soulier Syndrome Type C
Beta-defensin 119 Levels (defb119.13455.10.3)
Beta-klotho Levels
Betonicine Levels in Elite Athletes
Bifunctional 3-phosphoadenosine 5-phosphosulfate Synthase 1 Levels
Bifunctional Heparan Sulfate N-deacetylase/n-sulfotransferase 1 Levels
Bile Acid Conjugation Defect 1
Bile Acid Malabsorption
Bilirubin Concentration in Dolutegravir-treated Hiv Infection
Biomedical Quantitative Traits
Biotinidase Levels
Birk-barel Syndrome
Birth Length
Bladder Exstrophy-epispadias-cloacal Extrophy Complex
Blond Vs Non-blond Hair Color
Blood Cell Traits Latent Factor 15 (red Cell)
Bmp4-related Disorder
Bmpr2-related Disorder
Body Shape (principal Component Analysis)
Bone Mineral Density (paediatric, Lower Limb)
Bone Mineral Density (paediatric, Upper Limb)
Bone Morphogenetic Protein 7 Levels
Brachydactyly Type D
Brachydactyly Type E1
Brain Age (difference Between Predicted and Chronological Age)
Brain Age Gap From Gray Matter Volume
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →