Leigh disease
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.
Xref MGI. OMIM mapping confirmed by DO. [SN].
Exact Synonyms
Infantile necrotizing encephalomyelopathy
juvenile subacute necrotizing encephalomyelopathy
Leigh syndrome
Related Synonyms
subacute necrotizing encephalomyelopathy
class Information
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disease_ontology