bosch-boonstra-schaaf optic atrophy syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615722
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Genes

1 genes associated with the bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
NR2F1 nuclear receptor subfamily 2, group F, member 1