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
02397 DFNA13 deafness, autosomal dominant, type 13 (DFNA-13) 601868 AD 1 - COL11A2 - -
02871 DFNB53 deafness, autosomal recessive, type 53 (DFNB-53) 609706 AR - - COL11A2 - -
03676 FBCG2 fibrochondrogenesis, type 2 (FBCG-2) 614524 AD;AR - - COL11A2 - -
01569 OSMEDA dysplasia, otospondylomegaepiphyseal, autosomal dominant 184840 AD - - COL11A2 - -
00695 OSMEDB Otospondylomegaepiphyseal dysplasia, autosomal recessive 215150 AR 2 1 COL11A2, COL2A1 - -
02127 WZS Weissenbacher-Zweymuller syndrome (WZS) 277610 - - - COL11A2 - -
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