Summary Literature (0)

DOID:3652 - Leigh disease

Disease Ontology 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.

Synonyms: Infantile necrotizing encephalomyelopathy, Leigh syndrome, juvenile subacute necrotizing encephalomyelopathy, subacute necrotizing encephalomyelopathy,

Echinobase Genes : bcs1l, cox10, cox15, lrpprc, sdha


OMIM:

MIM:220111 - leigh syndrome, french canadian type; lsfc

MIM:256000 - leigh syndrome; ls

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee