All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03978 MMDD myopathy, due to myoadenylate deaminase deficiency (MMDD) 615511 1 1 AMPD1 - autosomal recessive