- OMIM ID
-
256000
- OMIM term:
- LEIGH SYNDROME; LS
- Alternative terms:
-
NECROTIZING ENCEPHALOPATHY, INFANTILE SUBACUTE, OF LEIGH; SNE LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY, INCLUDED
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX II DEFICIENCY, INCLUDED
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX III DEFICIENCY, INCLUDED
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX IV DEFICIENCY, INCLUDED
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX V DEFICIENCY, INCLUDED
- (∗) Location:
- 10q24.2 11p11.2 11q13.2 11q24.2 12p13.32 12q22 19p13.3 2q35 2q37.3 5p15.33 5q11.2 5q12.1 5q31.3 7q31.1 8q22.1 9q34.2
- (†) Associated OMIM genes:
- BCS1L C8ORF38 COX15 DLD FOXRED1 NDUFA10 NDUFA12 NDUFA2 NDUFA9 NDUFAF2 NDUFS3 NDUFS4 NDUFS7 NDUFS8 SDHA SURF1
- (‡) Associated MGI genes:
- Sod2 Surf1
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