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DO Term : Leigh disease [DOID:3652] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • UMLS_CUI:C0023264,
  • juvenile subacute necrotizing encephalomyelopathy,
  • OMIM:256000,
  • subacute necrotizing encephalomyelopathy,
  • ORDO:506,
  • Leigh syndrome,
  • SNOMEDCT_US_2023_03_01:29570005,
  • Infantile necrotizing encephalomyelopathy,
  • GARD:6877,
  • ICD10CM:G31.82,
  • 256000,
  • NCI:C84814,
  • MESH:D007888
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents