Search on: AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME 
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Descriptor English:   Autoimmune Lymphoproliferative Syndrome 
Descriptor Spanish:   Síndrome Linfoproliferativo Autoinmune 
Descriptor Portuguese:   Síndrome Linfoproliferativa Autoimune 
Synonyms English:   Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
Autoimmune Lymphoproliferative Syndrome Type 2B
Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B)
Canale Smith Syndrome
Caspase 8 Deficiency
Caspase-8 Deficiency  
Tree Number:   C15.604.515.138
C16.320.089
C20.111.288
C20.683.515.124
Definition English:   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. 
See Related English:   Antigens, CD95
Caspase 10
Caspase 8
Glucocorticoid-Induced TNFR-Related Protein
 
History Note English:   2010 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RA radiography RI radionuclide imaging
RT radiotherapy RH rehabilitation
SU surgery TH therapy
US ultrasonography UR urine
VE veterinary VI virology
Record Number:   53551 
Unique Identifier:   D056735 

Occurrence in VHL: 		 

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