Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:256000 - LEIGH SYNDROME; LS

Xenbase Genes: ndufv1, sdha, ndufs8, ndufs4, ndufs3, ndufs7, dld, bcs1l, ndufa2, cox15, ndufaf6, ndufa10, ndufa9, ndufa12, foxred1, surf1, cox10, ndufaf2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009723 - Leigh syndrome
MONDO:0016814 - maternally-inherited Leigh syndrome
MONDO:0016815 - obsolete Leigh syndrome with leukodystrophy
MONDO:0019083 - Leigh syndrome with cardiomyopathy

Disease Ontology (DO):
DOID:3652 - Leigh disease