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Summary Literature (0)
MIM:608358 - CONGENITAL MYOPATHY 7A, MYOSIN STORAGE, AUTOSOMAL DOMINANT; CMYO7A

Xenbase Genes: myh7l

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008409 - congenital myopathy 7A, myosin storage, autosomal dominant
MONDO:0012018 - obsolete myopathy, myosin storage, autosomal dominant
MONDO:0018889 - hyaline body myopathy

Disease Ontology (DO):
DOID:0111269 - autosomal dominant hyaline body myopathy