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Leigh syndrome

MONDO:0009723

Also known as: LS, LSS, Leigh disease, Leigh syndrome, Leigh syndrome spectrum

MONDO:
MONDO:0009723
Orphanet:
506
Rare disease96 associated genes

Description

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

Associated genes

+86 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.