Disease #02755 (MSMA (myopathy, myosin storage, autosomal dominant (MSMA)), OMIM:608358)

Official abbreviation MSMA
Name myopathy, myosin storage, autosomal dominant (MSMA)
OMIM ID 608358
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MYH7
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Disease features -
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Individuals

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00361997 - Sahin 2021, submitted - F no Turkey - - - - - MSMA Hypotonia HP:0001252 - MYH7 1 1 Ibrahim Sahin
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