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Disease Ontology Browser
Leigh disease (DOID:3652)
Alliance: disease page
Synonyms: Infantile necrotizing encephalomyelopathy; juvenile subacute necrotizing encephalomyelopathy; Leigh syndrome; subacute necrotizing encephalomyelopathy
Alt IDs: OMIM:256000, ICD10CM:G31.82, MESH:D007888, NCI:C84814, ORDO:506, UMLS_CUI:C0023264
Definition: A cytochrome-c oxidase deficiency 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 (11)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory