All diseases

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

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04583 CMS-9 myasthenic syndrome, congenital, type 9, associated with acetylcholine receptor deficiency (CMS-9) 616325 2 2 MUSK - autosomal recessive
01666 FADS akinesia, fetal, deformation sequence (FADS) 208150 19 19 DOK7, MUSK, RAPSN - -