Leigh disease (Disease)

Synonyms:Infantile necrotizing encephalomyelopathy, juvenile subacute necrotizing encephalomyelopathy, Leigh syndrome

Id:DOID:3652

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.

Results found

Linked to

	Label	Description
	SU001962 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001187 project
	SU001961 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001187 project
	SU001559 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001003 project
	SU001557 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001003 project
	SU001555 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001003 project
	SU001558 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001003 project
	SU001560 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001003 project
	SU001553 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001003 project
	SU001561 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001003 project
	SU001562 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001003 project

SU001962

Subject (Entity type)

A subject from Metabolomics produced as part of the PR001187 project

SU001961

Subject (Entity type)

A subject from Metabolomics produced as part of the PR001187 project

SU001559

Subject (Entity type)