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OMIM:160150 - MYOPATHY, CENTRONUCLEAR, 1; CNM1
DOID:14717 - centronuclear myopathy |
MONDO:0008048 - autosomal dominant centronuclear myopathy |
Human Disease Resources: OMIM
Xenbase Genes: myf6, mtmr14, dnm2
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DOID:14717 - centronuclear myopathy |
MONDO:0008048 - autosomal dominant centronuclear myopathy |