Search Ontology:
Human Disease
Leigh disease
- Term ID
- DOID:3652
- Synonyms
-
- Infantile necrotizing encephalomyelopathy
- juvenile subacute necrotizing encephalomyelopathy
- Leigh syndrome
- 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. (4)
- References
-
- GARD:6877
- ICD10CM:G31.82
- MESH:D007888
- Ontology
- Human Disease ( DOID:3652 )
- is a type of
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