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Descriptor en español: Artrogriposis
Descriptor artrogriposis
Término(s) alternativo(s) amioplasia congénita
artromiodisplasia congénita
miodistrofia fetal deformante
síndrome de Guerin-Stern
Nota de alcance: Flexión o contractura persistente de una articulación.
Descriptor en inglés: Arthrogryposis
Descriptor en portugués: Artrogripose
Descriptor en francés: Arthrogrypose
Término(s) alternativo(s): Amyoplasia Congenita
Arthrogryposes
Arthrogryposes, Congenital Multiple
Arthrogryposis Multiplex Congenita
Arthrogryposis Multiplex Congenita (AMC)
Arthrogryposis Multiplex Congenitas
Arthrogryposis Multiplex Congenitas (AMC)
Arthrogryposis, Congenital Multiple
Arthromyodysplasia, Congenital
Arthromyodysplasias, Congenital
Congenita, Arthrogryposis Multiplex
Congenita, Arthrogryposis Multiplex (AMC)
Congenital Arthromyodysplasia
Congenital Arthromyodysplasias
Congenital Multiple Arthrogryposes
Congenital Multiple Arthrogryposis
Congenitas, Arthrogryposis Multiplex
Congenitas, Arthrogryposis Multiplex (AMC)
Fibrous Ankylosis of Multiple Joints
Guerin Stern Syndrome
Guerin-Stern Syndrome
Guérin Stern Syndrome
Guérin-Stern Syndrome
Multiple Arthrogryposes, Congenital
Multiple Arthrogryposis, Congenital
Multiplex Congenita, Arthrogryposis
Multiplex Congenita, Arthrogryposis (AMC)
Multiplex Congenitas, Arthrogryposis
Multiplex Congenitas, Arthrogryposis (AMC)
Myodystrophia Fetalis Deformans
Otto Syndrome
Rocher Sheldon Syndrome
Rocher-Sheldon Syndrome
Rossi Syndrome
Syndrome, Guerin-Stern
Syndrome, Guérin-Stern
Syndrome, Otto
Syndrome, Rocher-Sheldon
Syndrome, Rossi
Código(s) jeráquico(s): C05.550.150
C05.651.102
C05.660.077
C16.131.621.077
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D001176
Nota de alcance: Persistent flexure or contracture of a joint.
Nota de indización: "persistent flexure or contracture of a joint"; 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: 65
Nota de historia: 65(63)
Identificador de DeCS: 1183
ID del Descriptor: D001176
Clasificación de la NLM: WE 304
Documentos indizados en la Biblioteca Virtual de Salud (BVS): Haga clic aquí para acceder a los documentos de la BVS
Fecha de establecimiento: 01/01/1965
Fecha de entrada: 01/01/1999
Fecha de revisión: 02/11/2018
Arthrogryposis - Concepto preferido
UI del concepto M0001754
Nota de alcance Persistent flexure or contracture of a joint.
Término preferido Arthrogryposis
Término(s) alternativo(s) Amyoplasia Congenita
Arthrogryposes
Arthrogryposes, Congenital Multiple
Arthrogryposis Multiplex Congenita
Arthrogryposis Multiplex Congenita (AMC)
Arthrogryposis Multiplex Congenitas
Arthrogryposis Multiplex Congenitas (AMC)
Arthrogryposis, Congenital Multiple
Arthromyodysplasia, Congenital
Arthromyodysplasias, Congenital
Congenita, Arthrogryposis Multiplex
Congenita, Arthrogryposis Multiplex (AMC)
Congenital Arthromyodysplasia
Congenital Arthromyodysplasias
Congenital Multiple Arthrogryposes
Congenital Multiple Arthrogryposis
Congenitas, Arthrogryposis Multiplex
Congenitas, Arthrogryposis Multiplex (AMC)
Fibrous Ankylosis of Multiple Joints
Guerin Stern Syndrome
Guerin-Stern Syndrome
Guérin Stern Syndrome
Guérin-Stern Syndrome
Multiple Arthrogryposes, Congenital
Multiple Arthrogryposis, Congenital
Multiplex Congenita, Arthrogryposis
Multiplex Congenita, Arthrogryposis (AMC)
Multiplex Congenitas, Arthrogryposis
Multiplex Congenitas, Arthrogryposis (AMC)
Myodystrophia Fetalis Deformans
Otto Syndrome
Rocher Sheldon Syndrome
Rocher-Sheldon Syndrome
Rossi Syndrome
Syndrome, Guerin-Stern
Syndrome, Guérin-Stern
Syndrome, Otto
Syndrome, Rocher-Sheldon
Syndrome, Rossi



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