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inborn mitochondrial myopathy

Disease Summary
Associated Targets (97)
Tbio

50

Tclin

29

Tchem

15

Tdark

3


Mondo Description Myopathy caused by mitochondrial abnormalities.
Disease Ontology Description A myopathy that is characterized by mitochondrial dysfunction.
Mondo Term and Equivalent IDs
MONDO:0009637:  inborn mitochondrial myopathy
GARD:0011956: 
MESH:D017240: 
NCIT:C101328: 
Orphanet:206966: 
UMLS:C0162670: