autoimmune lymphoproliferative syndrome type iv Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description RAS-associated autoimmune leukoproliferative disease (RALD) is a rare genetic disorder characterized by monocytosis, autoimmune cytopenias, lymphoproliferation, hepatosplenomegaly, and hypergammaglobulinemia. (Orphanet Rare Disease Ontology, Orphanet_268114)
External Link http://www.omim.org/entry/614470
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Genes

1 genes associated with the autoimmune lymphoproliferative syndrome type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog