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Descritor em português: Mucopolissacaridoses
Descritor em inglês: Mucopolysaccharidoses
Descritor em espanhol: Mucopolisacaridosis
Descritor mucopolisacaridosis
Nota de escopo: Grupo de enfermedades de almacenamiento lisosómico producida, cada una de ellas, por un déficit heredado de una enzima que participa en la degradación de los glicosaminoglicanos (mucopolisacáridos). Las enfermedades son progresivas y a menudo muestran un amplio espectro de gravedad clínica dependiendo del déficit enzimático.
Descritor em francês: Mucopolysaccharidoses
Termo(s) alternativo(s): Mucopolysaccharidosis
Código(s) hierárquico(s): C16.320.565.202.715
C16.320.565.595.600
C17.300.550.575
C18.452.648.202.715
C18.452.648.595.600
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D009083
Nota de escopo: Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.
Nota de indexação: lysosomal storage dis; types I through VII except V are available as main headings: V = MUCOPOLYSACCHARIDOSIS V see MUCOPOLYSACCHARIDOSIS I; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
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
Nota MeSH pública: 92; was MUCOPOLYSACCHARIDOSIS 1974-91
Nota Online: use MUCOPOLYSACCHARIDOSES to search MUCOPOLYSACCHARIDOSIS 1974-91
Nota histórica: 92; was MUCOPOLYSACCHARIDOSIS 1974-91
Identificador DeCS: 30388
ID do descritor: D009083
Documentos indexados na Biblioteca Virtual em Saúde (BVS): Clique aqui para acessar os documentos da BVS
Data de estabelecimento: 01/01/1974
Data de entrada: 01/01/1999
Data de revisão: 05/07/2006
Mucopolysaccharidoses - Conceito preferido
Identificador do conceito M0014167
Nota de escopo Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.
Termo preferido Mucopolysaccharidoses
Termo(s) alternativo(s) Mucopolysaccharidosis



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