Autoimmune Lymphoproliferative Syndrome
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.
Year introduced: 2010
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Subheadings:
Tree Number(s): C15.604.515.138, C16.320.089, C20.111.288, C20.683.515.124
MeSH Unique ID: D056735
Entry Terms:
- Autoimmune Lymphoproliferative Syndromes
- Lymphoproliferative Syndrome, Autoimmune
- Lymphoproliferative Syndromes, Autoimmune
- Syndrome, Autoimmune Lymphoproliferative
- Syndromes, Autoimmune Lymphoproliferative
- Canale Smith Syndrome
- Syndrome, Canale Smith
- Canale-Smith Syndrome
- Canale-Smith Syndromes
- Syndrome, Canale-Smith
- Syndromes, Canale-Smith
- Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant
- Autoimmune Lymphoproliferative Syndrome Type 2B
- Autoimmune Lymphoproliferative Syndrome, Type IIb
- Caspase-8 Deficiency
- Caspase-8 Deficiencies
- Deficiencies, Caspase-8
- Deficiency, Caspase-8
- Caspase 8 Deficiency
- Caspase 8 Deficiencies
- Deficiencies, Caspase 8
- Deficiency, Caspase 8
- Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B)
- Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
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