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| Descritor em português: | Imunodeficiência Combinada Severa | ||||||
| Descritor em inglês: | Severe Combined Immunodeficiency | ||||||
| Descritor em espanhol: |
Inmunodeficiencia Combinada Grave
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| Descritor em francês: | Immunodéficience combinée grave | ||||||
| Termo(s) alternativo(s): |
Bare Lymphocyte Syndrome Bare Lymphocyte Syndromes Combined Immunodeficiencies, Severe Combined Immunodeficiency, Severe Familial Reticuloendothelioses Familial Reticuloendotheliosis Immunodeficiencies, Severe Combined Immunodeficiency Syndrome, Severe Combined Immunodeficiency, Severe Combined Immunologic Deficiency, Severe Combined Lymphocyte Syndrome, Bare Lymphocyte Syndromes, Bare Omenn Syndrome Omenn's Syndrome Omenns Syndrome Reticuloendothelioses, Familial Reticuloendotheliosis, Familial Severe Combined Immune Deficiency Severe Combined Immunodeficiencies Severe Combined Immunodeficiency Syndrome Severe Combined Immunologic Deficiency Syndrome, Bare Lymphocyte Syndrome, Omenn Syndrome, Omenn's Syndromes, Bare Lymphocyte |
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| Código(s) hierárquico(s): |
C16.320.798.750 C16.614.815 C18.452.284.800 C20.673.795.750 |
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| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D016511 | ||||||
| Nota de escopo: | Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID). |
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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: |
Immunologic Deficiency Syndromes (1974-1991) |
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| Nota MeSH pública: | 1992 |
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| Nota histórica: | 1992 |
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| Versão alternativa: | SEVERE COMBINED IMMUNODEFIC |
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| Identificador DeCS: | 29820 | ||||||
| ID do descritor: | D016511 | ||||||
| Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||||
| Data de estabelecimento: | 01/01/1992 | ||||||
| Data de entrada: | 03/01/1991 | ||||||
| Data de revisão: | 20/06/2014 |
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Severe Combined Immunodeficiency
- Conceito preferido
Bare Lymphocyte Syndrome
- Relacionado, mas não mais amplo ou mais específico
Omenn Syndrome
- Mais específico
| Identificador do conceito |
M0025203 |
| Nota de escopo | Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID). |
| Termo preferido | Severe Combined Immunodeficiency |
| Termo(s) alternativo(s) |
Combined Immunodeficiencies, Severe Combined Immunodeficiency, Severe Immunodeficiencies, Severe Combined Immunodeficiency Syndrome, Severe Combined Immunodeficiency, Severe Combined Immunologic Deficiency, Severe Combined Severe Combined Immune Deficiency Severe Combined Immunodeficiencies Severe Combined Immunodeficiency Syndrome Severe Combined Immunologic Deficiency |
| Identificador do conceito |
M0025204 |
| Termo preferido | Bare Lymphocyte Syndrome |
| Termo(s) alternativo(s) |
Bare Lymphocyte Syndromes Lymphocyte Syndrome, Bare Lymphocyte Syndromes, Bare Syndrome, Bare Lymphocyte Syndromes, Bare Lymphocyte |
| Identificador do conceito |
M0520254 |
| Termo preferido | Omenn Syndrome |
| Termo(s) alternativo(s) |
Familial Reticuloendothelioses Familial Reticuloendotheliosis Omenn's Syndrome Omenns Syndrome Reticuloendothelioses, Familial Reticuloendotheliosis, Familial Syndrome, Omenn Syndrome, Omenn's |
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