All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01482 GDD dysplasia, gnathodiaphyseal (GDD) 166260 AD 16 15 ANO5 - -
03021 LGMD2L;LGMDR12 dystrophy, muscular, limb-girdle, type 2L (LGMD-2L) 611307 AR 39 37 ANO5 - -
03309 MMD3 dystrophy, muscular, Miyoshi, type 3 613319 AR 11 11 ANO5 - -
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