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| General Information | |||
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| Term | Leigh disease | ID (Ontology) | DOID:3652 (Human Disease) |
| 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. | ||
| Also Known As | "Infantile necrotizing encephalomyelopathy" ; "juvenile subacute necrotizing encephalomyelopathy" ; "Leigh syndrome" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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mitochondrial metabolism disease |__cytochrome-c oxidase deficiency disease |__Leigh disease 20 rec. |
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| Is a | cytochrome-c oxidase deficiency disease | ||
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External Crossreferences & Linkouts
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GARD:6877 ICD10CM:G31.82 MESH:D007888 MIM:256000 NCI:C84814 ORDO:506 SNOMEDCT_US_2023_03_01:29570005 UMLS_CUI:C0023264 |
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