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Disease Ontology Browser
Leigh disease (DOID:3652)
Synonyms: Infantile necrotizing encephalomyelopathy; juvenile subacute necrotizing encephalomyelopathy; Leigh syndrome; subacute necrotizing encephalomyelopathy
Alt IDs: OMIM:220111, OMIM:256000, ICD10CM:G31.82, MESH:D007888, NCI:C84814, ORDO:506, UMLS_CUI:C0023264
Definition: A mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity.

Disease References using Mouse Models (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory