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Autoimmune Lymphoproliferative Syndrome Type 4 (MONDO:0013767)

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

Overview

Category

syndromic disease

immune system disorder

Ontology ID

MONDO:0013767

Internal:14785

Synonyms

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

Mapped terms

DOID:0110117

GARD:0017262

MEDGEN:382434

OMIM:614470

Orphanet:268114

SCTID:723508002

UMLS:C2674723

Child terms

Unknown children.

Results

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