Details of Disease | DrugMAP

General Information of Disease (ID: DIS0IGW9)

Disease Name	Hyaline body myopathy
Synonyms	myosin storage myopathy
Disease Hierarchy	DIS2BIP8: Congenital nervous system disorder DISLSK9G: Congenital myopathy DISR8EC3: Qualitative or quantitative defects of beta-myosin heavy chain (MYH7) DIS0IGW9: Hyaline body myopathy

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
MYH7	TTNIMDP	Supportive	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
MYH7	OT4Z9T8N	Supportive	Autosomal dominant	[1]
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References

1	Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy. Neurology. 2004 May 11;62(9):1518-21. doi: 10.1212/01.wnl.0000123255.92062.37.