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(Q1394711)
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myofibrillar myopathy 3
No description defined
MFM3
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Statements
instance of
hereditary disorder
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rare disease
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disease
1 reference
stated in
Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy
subclass of
myofibrillar myopathy
0 references
genetic association
MYOT
1 reference
stated in
Mutations in myotilin cause myofibrillar myopathy
Identifiers
Google Knowledge Graph ID
/g/121g7347
0 references
OMIM ID
609200
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Sitelinks
Wikipedia
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Myofibrilläre Myopathie 3
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Wikiversity
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