All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05213 BAMS arhinia, choanal atresia, microphthalmia, Bosma type (BAMS) 603457 AD 51 51 SMCHD1 eyes;nose -
00083 FSHD2 dystrophy, muscular, facioscapulohumeral, type 2 (FSHD-2) 158901 - 146 118 DUX4, LRIF1, SMCHD1 - -
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