Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP8, and CASP10 proteins. Clinical features include LYMPHADENOPATHY; SPLENOMEGALY; and AUTOIMMUNITY.

Descriptor ID	D056735
MeSH Number(s)	C15.604.515.138 C16.320.089 C20.111.288 C20.683.515.124
Concept/Terms	Autoimmune Lymphoproliferative Syndrome Autoimmune Lymphoproliferative Syndrome Autoimmune Lymphoproliferative Syndromes Lymphoproliferative Syndrome, Autoimmune Lymphoproliferative Syndromes, Autoimmune Syndrome, Autoimmune Lymphoproliferative Syndromes, Autoimmune Lymphoproliferative Canale-Smith Syndrome Canale-Smith Syndromes Syndrome, Canale-Smith Syndromes, Canale-Smith Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant Canale Smith Syndrome Syndrome, Canale Smith Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant Autoimmune Lymphoproliferative Syndrome Type 2B Autoimmune Lymphoproliferative Syndrome Type 2B Caspase-8 Deficiency Caspase-8 Deficiencies Deficiencies, Caspase-8 Deficiency, Caspase-8 Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B) Autoimmune Lymphoproliferative Syndrome, Type IIb Caspase 8 Deficiency Caspase 8 Deficiencies Deficiencies, Caspase 8 Deficiency, Caspase 8

Below are MeSH descriptors whose meaning is more general than "Autoimmune Lymphoproliferative Syndrome".

Below are MeSH descriptors whose meaning is related to "Autoimmune Lymphoproliferative Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Autoimmune Lymphoproliferative Syndrome".