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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Autoimmune Lymphoproliferative Syndrome
Immune System Diseases > Immunoproliferative Disorders > Lymphoproliferative Disorders > Autoimmune Lymphoproliferative Syndrome
Hemic and Lymphatic Diseases > Lymphatic Diseases > Lymphoproliferative Disorders > Autoimmune Lymphoproliferative Syndrome
Immune System Diseases > Autoimmune Diseases > Autoimmune Lymphoproliferative Syndrome

Preferred term

Autoimmune Lymphoproliferative Syndrome  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant
  • Canale Smith Syndrome
  • Canale-Smith Syndrome
  • Canale-Smith Syndromes
  • Syndrome, Canale Smith
  • Syndrome, Canale-Smith
  • Syndromes, Canale-Smith

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.

History note

  • 2010

In other languages

URI

http://www.yso.fi/onto/mesh/D056735

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