Autoimmune lymphoproliferative syndrome type 4

RAS-associated autoimmune leukoproliferative disease (RALD) is a rare genetic disorder characterized by monocytosis, autoimmune cytopenias, lymphoproliferation, hepatosplenomegaly, and hypergammaglobulinemia.

Also known as: ALPS4, NRAS autoimmune lymphoproliferative syndrome, RALD, RAS-associated autoimmune leukoproliferative disease, RAS-associated autoimmune leukoproliferative disorder, RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic, autoimmune lymphoproliferative syndrome caused by mutation in NRAS, autoimmune lymphoproliferative syndrome, type 4

87 clinical trials for this condition and its sub-types, 3 tagged with Autoimmune lymphoproliferative syndrome type 4 itself.