Mesh term Autoimmune Lymphoproliferative Syndrome
Browse to parent terms:Autoimmune Diseases
Genetic Diseases, Inborn
Lymphoproliferative Disorders
Description
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.Search for this term in our Faculty Database
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