You are using an outdated browser. Please upgrade your browser to improve your experience.
mitochondrial encephalomyopathy
Disease Summary
Associated Targets (24)
Tbio
10
Tclin
8
Tchem
6
Mondo Description A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:890
MESH:D017237
SCTID:447292006
UMLS:C0162666
MONDO:0004675
High level summary of knowledge for a disease, including descriptions and datasource references.