Ha seleccionado la visión en Inglés
Descriptor en español: |
Mucopolisacaridosis
| ||||
Descriptor en inglés: | Mucopolysaccharidoses | ||||
Descriptor en portugués: | Mucopolissacaridoses | ||||
Descriptor en francés: | Mucopolysaccharidoses | ||||
Término(s) alternativo(s): |
Mucopolysaccharidosis |
||||
Código(s) jeráquico(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 alcance: | 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 indización: | 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 |
||||
Calificadores 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 Pública de MeSH: | 92; was MUCOPOLYSACCHARIDOSIS 1974-91 |
||||
Nota Online: | use MUCOPOLYSACCHARIDOSES to search MUCOPOLYSACCHARIDOSIS 1974-91 |
||||
Nota de historia: | 92; was MUCOPOLYSACCHARIDOSIS 1974-91 |
||||
Identificador de DeCS: | 30388 | ||||
ID del Descriptor: | D009083 | ||||
Documentos indizados en la Biblioteca Virtual de Salud (BVS): | Haga clic aquí para acceder a los documentos de la BVS | ||||
Fecha de establecimiento: | 01/01/1974 | ||||
Fecha de entrada: | 01/01/1999 | ||||
Fecha de revisión: | 05/07/2006 |
|
Mucopolysaccharidoses
- Concepto preferido
UI del concepto |
M0014167 |
Nota de alcance | 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. |
Término preferido | Mucopolysaccharidoses |
Término(s) alternativo(s) |
Mucopolysaccharidosis |
Queremos sus comentarios sobre el nuevo sitio web de DeCS / MeSH
Lo invitamos a completar una encuesta que no tomará más de 3 minutos.
Ir a la encuesta