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Descritor em português: Doenças Mitocondriais
Descritor em inglês: Mitochondrial Diseases
Descritor em espanhol: Enfermedades Mitocondriales
Descritor enfermedades mitocondriales
Termo(s) alternativo(s) deficiencias de fosforilación oxidativa
deficiencias mitocondriales de la cadena de transporte de electrones
enfermedad mitocondrial
Nota de escopo: Enfermedades causadas por un funcionamiento anómalo de la MITOCONDRIA, que puede deberse a mutaciones, adquiridas o heredadas, en el ADN mitocondrial o en genes del núcleo encargados de codificar componentes mitocondriales. Estas enfermedades tambien pueden ser resultado de disfunciones mitocondriales adquiridas, derivadas de efectos adversos de drogas, infecciones u otras causas ambientales.
Descritor em francês: Maladies mitochondriales
Termo(s) alternativo(s): Deficiencies, Oxidative Phosphorylation
Deficiencies, Respiratory Chain
Deficiency, Oxidative Phosphorylation
Deficiency, Respiratory Chain
Disease, Mitochondrial
Disorder, Mitochondrial
Disorders, Mitochondrial
Electron Transport Chain Deficiencies, Mitochondrial
Mitochondrial Disease
Mitochondrial Disorder
Mitochondrial Disorders
Mitochondrial Electron Transport Chain Deficiencies
Mitochondrial Respiratory Chain Deficiencies
Oxidative Phosphorylation Deficiencies
Oxidative Phosphorylation Deficiency
Phosphorylation Deficiencies, Oxidative
Phosphorylation Deficiency, Oxidative
Respiratory Chain Deficiencies, Mitochondrial
Respiratory Chain Deficiency
Código(s) hierárquico(s): C18.452.660
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D028361
Nota de escopo: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
Nota de indexação: general or unspecified; prefer specifics
Qualificadores permitidos: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
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
Indexação Anterior: Mitochondria (1987-2001)
Mitochondrial Myopathies (1992-2001)
Nota MeSH pública: 2002; see MITOCHONDRIAL MYOPATHIES 2000-2001
Nota histórica: 2002; use MITOCHONDRIAL MYOPATHIES 2000-2001
Versão alternativa: MITOCHONDRIAL DIS
Identificador DeCS: 36033
ID do descritor: D028361
Classificação da NLM: WD 200.5.M6
Documentos indexados na Biblioteca Virtual em Saúde (BVS): Clique aqui para acessar os documentos da BVS
Data de estabelecimento: 01/01/2002
Data de entrada: 03/08/2001
Mitochondrial Diseases - Conceito preferido
Identificador do conceito M0335637
Nota de escopo Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
Termo preferido Mitochondrial Diseases
Termo(s) alternativo(s) Disease, Mitochondrial
Disorder, Mitochondrial
Disorders, Mitochondrial
Mitochondrial Disease
Mitochondrial Disorder
Mitochondrial Disorders
Oxidative Phosphorylation Deficiencies - Mais específico
Identificador do conceito M0382031
Termo preferido Oxidative Phosphorylation Deficiencies
Termo(s) alternativo(s) Deficiencies, Oxidative Phosphorylation
Deficiency, Oxidative Phosphorylation
Oxidative Phosphorylation Deficiency
Phosphorylation Deficiencies, Oxidative
Phosphorylation Deficiency, Oxidative
Respiratory Chain Deficiencies, Mitochondrial - Mais específico
Identificador do conceito M0382030
Termo preferido Respiratory Chain Deficiencies, Mitochondrial
Termo(s) alternativo(s) Deficiencies, Respiratory Chain
Deficiency, Respiratory Chain
Mitochondrial Respiratory Chain Deficiencies
Respiratory Chain Deficiency
Electron Transport Chain Deficiencies, Mitochondrial - Mais específico
Identificador do conceito M0387124
Termo preferido Electron Transport Chain Deficiencies, Mitochondrial
Termo(s) alternativo(s) Mitochondrial Electron Transport Chain Deficiencies



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