Details of Disease | DrugMAP

General Information of Disease (ID: DISR9FAQ)

Disease Name	Miyoshi muscular dystrophy 3
Synonyms	Miyoshi myopathy 3; distal anoctaminopathy; MMD3; Miyoshi muscular dystrophy type 3; Miyoshi muscular dystrophy 3
Disease Hierarchy	DIS3O1UR: Miyoshi myopathy DISR9FAQ: Miyoshi muscular dystrophy 3
Disease Identifiers	MONDO ID MONDO_0013222 MESH ID C567645 UMLS CUI C2750076 OMIM ID 613319 MedGen ID 413750 Orphanet ID 399096 SNOMED CT ID 783166000

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
ANO5	OTOW8R6H	Strong	Autosomal recessive	[1]
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References

1	[Hyperviscosity syndrome in plasma cell dyscrasia]. Harefuah. 1979 Feb 1;96(3):161-3.