disease has feature Strabismus Leigh syndrome https://github.com/monarch-initiative/mondo/issues/6090 https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/leigh_disease https://www.malacards.org/card/leigh_syndrome_nuclear Orphanet:506 Leigh disease MONDO:0009723 Leigh's disease subacute necrotizing encephalopathy NANDO:1200175 NCIT:C84814 Leigh syndrome due to mitochondrial Complex 5 deficiency LSS NANDO:2200527 OMIM:256000 Leigh syndrome due to mitochondrial Complex 1 deficiency Leigh syndrome due to mitochondrial Complex 4 deficiency UMLS:C2931891 LS infantile subacute necrotizing encephalopathy Leigh syndrome GARD:0006877 Leigh syndrome due to mitochondrial Complex 3 deficiency MESH:D007888 necrotizing encephalopathy, infantile Subacute, of Leigh icd11.foundation:672871576 Leigh syndrome due to mitochondrial Complex 2 deficiency ICD9:330.8 MedDRA:10062950 Leigh syndrome spectrum SNE MEDGEN:419518 SCTID:29570005 ICD10CM:G31.82 DOID:3652 A progressive neurological disease defined by specific neuropathological features associating brainstem and basal ganglia lesions. NORD:1355 Leigh's necrotizing encephalopathy obsolete neuro-ophthalmological disease mitochondrial oxidative phosphorylation disorder hereditary peripheral neuropathy supranuclear oculomotor palsy