Concept information
Preferred term
Autoimmune Lymphoproliferative Syndrome
Type
-
mesh:Descriptor
Definition
- 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. Autoimmune lymphoproliferative syndrome due to mutations in CASPASE 8 gene.
Broader concept
Entry terms
- Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant
- Canale Smith Syndrome
- Canale-Smith Syndrome
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
SLPA
-
Syndrome de Canale-Smith
-
Syndrome lymphoprolifératif auto-immun
-
Syndrome lymphoprolifératif avec autoimmunité
URI
http://data.loterre.fr/ark:/67375/JVR-XD1F4DRZ-Q
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