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MIM:618823 - CONGENITAL MYOPATHY 9B, PROXIMAL, WITH MINICORE LESIONS; CMYP9B
Xenbase Genes:
Human Disease Resource: OMIM
MONDO:0032937 - myopathy, congenital proximal, with minicore lesions |
DOID:0081344 - congenital myopathy 9B |
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MONDO:0032937 - myopathy, congenital proximal, with minicore lesions |
DOID:0081344 - congenital myopathy 9B |