bare lymphocyte syndrome, type ii, complementation group d Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/209920
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Genes

1 genes associated with the bare lymphocyte syndrome, type ii, complementation group d phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
RFXAP regulatory factor X-associated protein