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DOID:3652 - Leigh disease
Disease Ontology 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.
Synonyms: Infantile necrotizing encephalomyelopathy, juvenile subacute necrotizing encephalomyelopathy, Leigh syndrome, subacute necrotizing encephalomyelopathy
Echinobase Genes
:
bcs1l,
cox10,
cox15,
lrpprc,
sdha
| MIM:220111 - leigh syndrome, french canadian type; lsfc |
| MIM:256000 - leigh syndrome; ls |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee