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
04583 CMS9 myasthenic syndrome, congenital, type 9, associated with acetylcholine receptor deficiency (CMS-9) 616325 AR 3 2 MUSK - autosomal recessive
01666 FADS akinesia, fetal, deformation sequence (FADS) - - 41 40 DOK7, MUSK, NUP88, RAPSN - -
05866 FADS1 akinesia, fetal, deformation sequence, type 1 (FADS1) 208150 AR - - MUSK - -
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