Search Ontology:
Human Disease

Leigh disease

Term ID
DOID:3652
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
  • MIM:256000
  • NCI:C84814
  • ORDO:506
  • SNOMEDCT_US_2023_03_01:29570005
  • UMLS_CUI:C0023264
Ontology
Human Disease   ( DOID:3652 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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