?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/616079
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Genes

1 genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ITM2B integral membrane protein 2B