All diseases

4 entries on 1 page. Showing entries 1 - 4.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00105 ACG-1B achondrogenesis, type IB (ACG-1B) 600972 1 1 SLC26A2 - -
00106 AO-2 atelosteogenesis, type II (AO-2, De la Chapelle dysplasia) 256050 0 0 SLC26A2 - -
00072 DTD dysplasia, diastrophic (DTD) 222600 0 0 SLC26A2 - -
00107 EDM-4 dysplasia, epiphyseal, multiple, type 4 (EDM-4) 226900 0 0 SLC26A2 - -