Pesquisa
Descritor em português: Artrogripose
Descritor em inglês: Arthrogryposis
Descritor em espanhol: Artrogriposis
Descritor artrogriposis
Termo(s) alternativo(s) amioplasia congénita
artromiodisplasia congénita
miodistrofia fetal deformante
síndrome de Guerin-Stern
Nota de escopo: Flexión o contractura persistente de una articulación.
Descritor em francês: Arthrogrypose
Termo(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) hierárquico(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 escopo: Persistent flexure or contracture of a joint.
Nota de indexação: "persistent flexure or contracture of a joint"; 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: 65
Nota histórica: 65(63)
Identificador DeCS: 1183
ID do descritor: D001176
Classificação da NLM: WE 304
Documentos indexados na Biblioteca Virtual em Saúde (BVS): Clique aqui para acessar os documentos da BVS
Data de estabelecimento: 01/01/1965
Data de entrada: 01/01/1999
Data de revisão: 02/11/2018
Arthrogryposis - Conceito preferido
Identificador do conceito M0001754
Nota de escopo Persistent flexure or contracture of a joint.
Termo preferido Arthrogryposis
Termo(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



Queremos a sua opinião sobre o novo sitio web do DeCS/MeSH

Convidamos-lhe a responder a uma pesquisa que não levará mais que 3 minutos


Ir para pesquisa