All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05479 ACG achondrogenesis (ACG) - - 1 1 COL2A1, SLC26A2, TRIP11 - -
00105 ACG-1B achondrogenesis, type IB (ACG-1B) 600972 - 1 3 SLC26A2 - -
00106 AO-2 atelosteogenesis, type II (AO-2, De la Chapelle dysplasia) 256050 - 1 4 SLC26A2 - -
00072 DTD dysplasia, diastrophic (DTD) 222600 - 0 0 SLC26A2 - -
00107 EDM-4 dysplasia, epiphyseal, multiple, type 4 (EDM-4) 226900 - 0 6 SLC26A2 - -
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