Visão selecionada em Inglês
Descritor em português: | Deficiência Múltipla de Carboxilase | ||||||
Descritor em inglês: | Multiple Carboxylase Deficiency | ||||||
Descritor em espanhol: |
Deficiencia Múltiple de Carboxilasa
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Descritor em francês: | Déficit multiple en carboxylases | ||||||
Termo(s) alternativo(s): |
Carboxylase Deficiencies, Combined Carboxylase Deficiencies, Multiple Carboxylase Deficiency, Combined Carboxylase Deficiency, Multiple Combined Carboxylase Deficiencies Combined Carboxylase Deficiency Deficiencies, Combined Carboxylase Deficiencies, Multiple Carboxylase Deficiency, Combined Carboxylase Deficiency, Multiple Carboxylase Multiple Carboxylase Deficiencies |
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Código(s) hierárquico(s): |
C16.320.565.100.620 C16.320.565.202.720 C18.452.648.100.620 C18.452.648.202.720 |
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Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D009100 | ||||||
Nota de escopo: | A deficiency in the activities of biotin-dependent enzymes (propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, and PYRUVATE CARBOXYLASE) due to one of two defects in BIOTIN metabolism. The neonatal form is due to HOLOCARBOXYLASE SYNTHETASE DEFICIENCY. The late-onset form is due to BIOTINIDASE DEFICIENCY. |
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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: |
specific enzyme (1966-1974) specific enzyme/deficiency (1975-1986) |
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Nota MeSH pública: | 87 |
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Nota histórica: | 87 |
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Versão alternativa: | MULTIPLE CARBOXYLASE DEFIC |
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Veja também os descritores: |
Biotin
MeSH | ||||||
Identificador DeCS: | 19252 | ||||||
ID do descritor: | D009100 | ||||||
Documentos indexados na Biblioteca Virtual em Saúde (BVS): | Clique aqui para acessar os documentos da BVS | ||||||
Data de estabelecimento: | 01/01/1987 | ||||||
Data de entrada: | 18/04/1986 | ||||||
Data de revisão: | 05/07/2006 |
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Multiple Carboxylase Deficiency
- Conceito preferido
Identificador do conceito |
M0014194 |
Nota de escopo | A deficiency in the activities of biotin-dependent enzymes (propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, and PYRUVATE CARBOXYLASE) due to one of two defects in BIOTIN metabolism. The neonatal form is due to HOLOCARBOXYLASE SYNTHETASE DEFICIENCY. The late-onset form is due to BIOTINIDASE DEFICIENCY. |
Termo preferido | Multiple Carboxylase Deficiency |
Termo(s) alternativo(s) |
Carboxylase Deficiencies, Combined Carboxylase Deficiencies, Multiple Carboxylase Deficiency, Combined Carboxylase Deficiency, Multiple Combined Carboxylase Deficiencies Combined Carboxylase Deficiency Deficiencies, Combined Carboxylase Deficiencies, Multiple Carboxylase Deficiency, Combined Carboxylase Deficiency, Multiple Carboxylase Multiple Carboxylase Deficiencies |
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