Visão selecionada em Inglês
| Descritor em português: | Síndrome Linfoproliferativa Autoimune | ||||||
| Descritor em inglês: | Autoimmune Lymphoproliferative Syndrome | ||||||
| Descritor em espanhol: |
Síndrome Linfoproliferativo Autoinmune
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| Descritor em francês: | Syndrome lymphoprolifératif avec auto-immunité | ||||||
| Termo(s) alternativo(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 Autoimmune Lymphoproliferative Syndromes Canale Smith Syndrome Canale-Smith Syndrome Canale-Smith Syndromes Caspase 8 Deficiencies Caspase 8 Deficiency Caspase-8 Deficiencies Caspase-8 Deficiency Deficiencies, Caspase 8 Deficiencies, Caspase-8 Deficiency, Caspase 8 Deficiency, Caspase-8 Lymphoproliferative Syndrome, Autoimmune Lymphoproliferative Syndromes, Autoimmune Syndrome, Autoimmune Lymphoproliferative Syndrome, Canale Smith Syndrome, Canale-Smith Syndromes, Autoimmune Lymphoproliferative Syndromes, Canale-Smith |
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| Código(s) hierárquico(s): |
C15.604.515.138 C16.320.089 C20.111.288 C20.683.515.124 |
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| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D056735 | ||||||
| Nota de escopo: | 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. |
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| Qualificadores permitidos: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Indexação Anterior: |
Autoimmune Diseases (1997-2009) Lymphoproliferative Disorders (1983-2009) |
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| Nota MeSH pública: | 2010 |
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| Nota histórica: | 2010 |
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| Veja também os descritores: |
Caspase 10
MeSH Caspase 8 MeSH Glucocorticoid-Induced TNFR-Related Protein MeSH fas Receptor MeSH | ||||||
| Identificador DeCS: | 53551 | ||||||
| ID do descritor: | D056735 | ||||||
| Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||||
| Data de estabelecimento: | 01/01/2010 | ||||||
| Data de entrada: | 06/07/2009 | ||||||
| Data de revisão: | 17/07/2017 |
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Autoimmune Lymphoproliferative Syndrome
- Conceito preferido
Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
- Mais específico
Autoimmune Lymphoproliferative Syndrome Type 2B
- Mais específico
| Identificador do conceito |
M0528916 |
| Nota de escopo | 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. |
| Termo preferido | Autoimmune Lymphoproliferative Syndrome |
| Termo(s) alternativo(s) |
Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant Autoimmune Lymphoproliferative Syndromes Canale Smith Syndrome Canale-Smith Syndrome Canale-Smith Syndromes Lymphoproliferative Syndrome, Autoimmune Lymphoproliferative Syndromes, Autoimmune Syndrome, Autoimmune Lymphoproliferative Syndrome, Canale Smith Syndrome, Canale-Smith Syndromes, Autoimmune Lymphoproliferative Syndromes, Canale-Smith |
| Identificador do conceito |
M0529217 |
| Termo preferido | Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant |
| Identificador do conceito |
M0528917 |
| Nota de escopo | Autoimmune lymphoproliferative syndrome due to mutations in CASPASE 8 gene. |
| Termo preferido | Autoimmune Lymphoproliferative Syndrome Type 2B |
| Termo(s) alternativo(s) |
Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B) Autoimmune Lymphoproliferative Syndrome, Type IIb Caspase 8 Deficiencies Caspase 8 Deficiency Caspase-8 Deficiencies Caspase-8 Deficiency Deficiencies, Caspase 8 Deficiencies, Caspase-8 Deficiency, Caspase 8 Deficiency, Caspase-8 |
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