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Autoimmune lymphoproliferative syndrome type 4
rareRAS-associated autoimmune leukoproliferative disease (RALD) is a rare genetic disorder characterized by monocytosis, autoimmune cytopenias, lymphoproliferation, hepatosplenomegaly, and hypergammaglobulinemia.
- Identifiers
- MONDO:0013767 OMIM:614470Orphanet:268114
- Causal genes
- NRAS
- Also known as
- ALPS4 · autoimmune lymphoproliferative syndrome caused by mutation in NRAS · NRAS autoimmune lymphoproliferative syndrome · RALD · RAS-associated autoimmune leukoproliferative disease
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