Disease #00015

Official abbreviation LS
Name Leigh syndrome due to mitochondrial complex 1 deficiency, 256000 (3)
OMIM ID 256000
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 20 genes BCS1L, COX10, COX15, FOXRED1, MT-ATP6, MT-TK, MT-TV, MT-TW, NDUFA10, NDUFA12, NDUFA2, NDUFA9, NDUFAF2, NDUFAF6, NDUFS3, NDUFS4, NDUFS7, NDUFS8, SDHA, SURF1
Associated tissues -
Disease features -
Remarks -