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MIM:181430 - MOVED TO 608358
Xenbase Genes: myh7
Human Disease Resource: OMIM
MONDO:0008409 - congenital myopathy 7A, myosin storage, autosomal dominant |
DOID:0060253 - scapuloperoneal myopathy |
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MONDO:0008409 - congenital myopathy 7A, myosin storage, autosomal dominant |
DOID:0060253 - scapuloperoneal myopathy |