All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01212 BDD brachydactyly, type D (BD-D) 113200 AD 3 3 HOXD13 - -
01213 BDE1 brachydactyly type E1 (BD-E1) 113300 AD 1 1 HOXD13 - -
02973 BDSD brachydactyly-syndactyly syndrome (BDSD) 610713 - - - HOXD13 - -
01573 SDTY5 syndactyly, type V, with metacarpal and metatarsal fusion (SDTY-5) 186300 AD - - HOXD13 - -
01572 SPD1;SDTY2 synpolydactyly, type 1 (SPD-1, syndactyly type II (SDTY-2)) 186000 AD - - HOXD13 - -
01595 VATER vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, radial or renal dysplasia, assoc. (VATER) 192350 - 1 1 HOXD13 - -
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