leigh syndrome due to mitochondrial complex 1 deficiency Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/256000
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Genes

1 genes associated with the leigh syndrome due to mitochondrial complex 1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
NDUFA12 NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12