General Information of Disease (ID: DIS4AWOQ)

Disease Name Myopathy, sarcoplasmic body
Disease Hierarchy
DISOWG27: Myopathy
DIS4AWOQ: Myopathy, sarcoplasmic body
Disease Identifiers
MONDO ID
MONDO_0859530
UMLS CUI
C5830362
OMIM ID
620286
MedGen ID
1840998

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
MB OTYWYL2D Strong Autosomal dominant [1]
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References

1 Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions. Nat Commun. 2019 Mar 27;10(1):1396. doi: 10.1038/s41467-019-09111-2.