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Leigh Syndrome (MONDO:0009723)

A progressive neurological disease defined by specific neuropathological features associating brainstem and basal ganglia lesions.

Overview

Category

Ontology ID

Internal:10936

Synonyms

LSS

Leigh disease

Leigh syndrome

Leigh syndrome spectrum

Leigh's disease

infantile subacute necrotizing encephalopathy

Leigh syndrome due to mitochondrial Complex 1 deficiency

Leigh syndrome due to mitochondrial Complex 2 deficiency

Leigh syndrome due to mitochondrial Complex 3 deficiency

Leigh syndrome due to mitochondrial Complex 4 deficiency

Leigh syndrome due to mitochondrial Complex 5 deficiency

Leigh's necrotizing encephalopathy

SNE

necrotizing encephalopathy, infantile Subacute, of Leigh

subacute necrotizing encephalopathy

Mapped terms

DOID:3652

GARD:0006877

ICD10CM:G31.82

ICD9:330.8

MEDGEN:419518

MESH:D007888

MedDRA:10062950

NANDO:1200175

NANDO:2200527

NCIT:C84814

NORD:1355

OMIM:256000

Orphanet:506

SCTID:29570005

UMLS:C2931891

icd11.foundation:672871576

Child terms