myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/613076
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Genes

1 genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
GFER growth factor, augmenter of liver regeneration