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Autoimmune Lymphoproliferative Syndrome MeSH Descriptor Data 2022


MeSH Heading
Autoimmune Lymphoproliferative Syndrome
Tree Number(s)
C15.604.515.138
C16.320.089
C20.111.288
C20.683.515.124
Unique ID
D056735
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D056735
Scope Note
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.
Entry Term(s)
Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
Autoimmune Lymphoproliferative Syndrome Type 2B
Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B)
Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant
Autoimmune Lymphoproliferative Syndrome, Type IIb
Canale Smith Syndrome
Canale-Smith Syndrome
Caspase 8 Deficiency
Caspase-8 Deficiency
Previous Indexing
Autoimmune Diseases (1997-2009)
Lymphoproliferative Disorders (1983-2009)
See Also
Caspase 10
Caspase 8
fas Receptor
Glucocorticoid-Induced TNFR-Related Protein
Public MeSH Note
2010
History Note
2010
Date Established
2010/01/01
Date of Entry
2009/07/06
Revision Date
2017/07/17
Autoimmune Lymphoproliferative Syndrome Preferred
Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant Narrower
Autoimmune Lymphoproliferative Syndrome Type 2B Narrower
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