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Autoimmune lymphoproliferative syndrome

rare

Autoimmune lymphoproliferative syndrome (ALPS) is a rare, inherited disorder characterized by non-malignant lymphoproliferation, multilineage cytopenias, and a lifelong increased risk of Hodgkin's and non-Hodgkin's lymphoma.

Identifiers
MONDO:0017979 Orphanet:3261
Part of
Autoimmune diseaseLymphoproliferative syndromeNeoplastic syndromeType IV hypersensitivity disease
Also known as
ALPS · ALPS (autoimmune lymphoproliferative syndrome) · autoimmune lymphoproliferative syndrome type 1, autosomal dominant · Canale-Smith syndrome · FAS deficiency

Subtypes

All diseases Rare only
Disease Subtypes
Castleman-Kojima disease
FAS-related autoimmune lymphoproliferative immune disorder
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
Autoimmune lymphoproliferative syndrome type 1
Autoimmune lymphoproliferative syndrome type 2A
Autoimmune lymphoproliferative syndrome type 2B
Autoimmune lymphoproliferative syndrome type 4
Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD
Type 3 autoimmune lymphoproliferative syndrome

Rare disease

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