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
05554 CMYO3;RSMD1 myopathy, congenital, type 3, with rigid spine 602771 AR 2 2 SEPN1 - autosomal recessive
02439 RSMD dystrophy, muscular, rigid spine (RSMD) - - 126 126 SEPN1 - -
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