Autoimmune lymphoproliferative syndrome
MONDO:0017979Autoimmune 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.
Also known as: ALPS, ALPS (autoimmune lymphoproliferative syndrome), Canale-Smith syndrome, FAS deficiency, autoimmune lymphoproliferative syndrome type 1, autosomal dominant
91 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Autoimmune lymphoproliferative syndrome type 4
(3)
FAS-related autoimmune lymphoproliferative syndrome
(2)
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
(1)
Autoimmune lymphoproliferative syndrome type 1
(0)
Autoimmune lymphoproliferative syndrome type 2A
(0)
Autoimmune lymphoproliferative syndrome type 2B
(0)
Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD
(0)
Castleman-Kojima disease
(0)
Type 3 autoimmune lymphoproliferative syndrome
(0)