OBO ID: DOID:3652
Term Name: Leigh disease Search Ontology:
Synonyms:
  • Infantile necrotizing encephalomyelopathy
  • juvenile subacute necrotizing encephalomyelopathy
  • Leigh syndrome
  • subacute necrotizing encephalomyelopathy
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
  • NCI:C84814
  • OMIM:256000
  • ORDO:506
  • SNOMEDCT_US_2023_03_01:29570005
  • UMLS_CUI:C0023264
Ontology: Human Disease   ( DOID:3652 )
Relationships
is a type of:
OTHER Leigh disease PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS (1)
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