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Descritor em português: Osteocondrodisplasias
Descritor em inglês: Osteochondrodysplasias
Descritor em espanhol: Osteocondrodisplasias
Descritor osteocondrodisplasias
Termo(s) alternativo(s) discondroplasias
displasia epifisiaria múltiple
hiperostosis cortical generalizada
síndrome de Melnick-Needles
síndrome de Schwartz-Jample
Nota de escopo: Desarrollo anormal del cartílago y el hueso.
Descritor em francês: Ostéochondrodysplasies
Termo(s) alternativo(s): Chondrodystrophic Myotonia
Chondrodystrophy, Myotonic
Dyschondroplasia
Dyschondroplasias
Dysplasia, Spondyloepiphyseal
Endosteal Hyperostosis, Autosomal Recessive
Hyperostosis Corticalis Generalisata
Hyperphosphatasemia Tarda
Late Onset Spondyloepiphyseal Dysplasia
Late Spondyloepiphyseal Dysplasia
Late-Onset Spondyloepiphyseal Dysplasia
Melnick Needles Osteodysplasty
Melnick Needles Syndrome
Melnick-Needles Osteodysplasty
Melnick-Needles Syndrome
Multiple Epiphyseal Dysplasia
Myotonia, Chondrodystrophic
Myotonic Chondrodystrophy
Myotonic Myopathy, Dwarfism, Chondrodystrophy, And Ocular And Facial Abnormalities
Osteochondrodysplasia
Osteodysplasty of Melnick and Needles
Osteodysplasty, Melnick-Needles
SED Tarda
SED, X-Linked
SEDT, X-Linked
SJA Syndrome
Schwartz Jampel Aberfeld syndrome
Schwartz Jampel Syndrome
Schwartz Jampel Syndrome, Type 1
Schwartz-Jampel Syndrome
Schwartz-Jampel Syndrome, Type 1
Schwartz-Jampel-Aberfeld Syndrome
Sost Sclerosing Bone Dysplasia
Sost-Related Sclerosing Bone Dysplasia
Spondylo-Epimetaphyseal Dysplasia With Myotonia
Spondyloepiphyseal Dysplasia
Spondyloepiphyseal Dysplasia Tarda, X Linked
Spondyloepiphyseal Dysplasia Tarda, X-Linked
Spondyloepiphyseal Dysplasia, Late
Spondyloepiphyseal Dysplasia, Late-Onset
Syndrome, Schwartz-Jampel-Aberfeld
Van Buchem Disease
X Linked SED
X Linked SEDT
X Linked Spondyloepiphyseal Dysplasia Tarda
X-Linked SED
X-Linked SEDT
X-Linked Spondyloepiphyseal Dysplasia Tarda
Código(s) hierárquico(s): C05.116.099.708
C16.320.728
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D010009
Nota de escopo: Abnormal development of cartilage and bone.
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: Bone Diseases (1966-1969)
Bone Diseases, Developmental (1970-1984)
Nota MeSH pública: 85; DYSCHONDRODYSPLASIAS was heading DYSCHONDROPLASIA 1963-84; SPONDYLEPIPHYSEAL DYSPLASIA was see MUCOPOLYSACCHARIDOSIS 4 1980-84, was see ECCENTROOSTEOCHONDRODYSPLASIA 1968-79
Nota Online: use OSTECHONDRODYSPLASIAS to search DYSCHONDROPLASIAS 1966-84; use MUCOPOLYSACCHARIDOSIS 4 to search SPONDYLOEPIPHYSEAL DYSPLASIA 1968-84
Nota histórica: 85; DYSCHONDRODYSPLASIAS was heading DYSCHONDROPLASIA 1963-84; SPONDYLOEPIPHYSEAL DYSPLASIA was see MUCOPOLYSACCHARIDOSIS 4 1980-84, was see ECCENTROOSTEOCHONDRODYSPLASIA 1968-79
Identificador DeCS: 10187
ID do descritor: D010009
Classificação da NLM: WE 250
Documentos indexados na Biblioteca Virtual em Saúde (BVS): Clique aqui para acessar os documentos da BVS
Data de estabelecimento: 01/01/1985
Data de entrada: 06/04/1984
Data de revisão: 10/10/2018
Osteochondrodysplasias - Conceito preferido
Identificador do conceito M0015525
Nota de escopo Abnormal development of cartilage and bone.
Termo preferido Osteochondrodysplasias
Termo(s) alternativo(s) Osteochondrodysplasia
Melnick-Needles Syndrome - Mais específico
Identificador do conceito M0015523
Termo preferido Melnick-Needles Syndrome
Termo(s) alternativo(s) Melnick Needles Osteodysplasty
Melnick Needles Syndrome
Melnick-Needles Osteodysplasty
Osteodysplasty of Melnick and Needles
Osteodysplasty, Melnick-Needles
Multiple Epiphyseal Dysplasia - Relacionado, mas não mais amplo ou mais específico
Identificador do conceito M0015524
Termo preferido Multiple Epiphyseal Dysplasia
Myotonic Chondrodystrophy - Relacionado, mas não mais amplo ou mais específico
Identificador do conceito M0533083
Termo preferido Myotonic Chondrodystrophy
Termo(s) alternativo(s) Chondrodystrophic Myotonia
Chondrodystrophy, Myotonic
Myotonia, Chondrodystrophic
Myotonic Myopathy, Dwarfism, Chondrodystrophy, And Ocular And Facial Abnormalities
SJA Syndrome
Schwartz Jampel Aberfeld syndrome
Schwartz Jampel Syndrome
Schwartz-Jampel Syndrome
Schwartz-Jampel-Aberfeld Syndrome
Spondylo-Epimetaphyseal Dysplasia With Myotonia
Syndrome, Schwartz-Jampel-Aberfeld
Spondyloepiphyseal Dysplasia - Mais específico
Identificador do conceito M0015527
Termo preferido Spondyloepiphyseal Dysplasia
Termo(s) alternativo(s) Dysplasia, Spondyloepiphyseal
Spondyloepiphyseal Dysplasia Tarda, X-Linked - Mais específico
Identificador do conceito M0562747
Termo preferido Spondyloepiphyseal Dysplasia Tarda, X-Linked
Termo(s) alternativo(s) Late Onset Spondyloepiphyseal Dysplasia
Late Spondyloepiphyseal Dysplasia
Late-Onset Spondyloepiphyseal Dysplasia
SED Tarda
SED, X-Linked
SEDT, X-Linked
Spondyloepiphyseal Dysplasia Tarda, X Linked
Spondyloepiphyseal Dysplasia, Late
Spondyloepiphyseal Dysplasia, Late-Onset
X Linked SED
X Linked SEDT
X Linked Spondyloepiphyseal Dysplasia Tarda
X-Linked SED
X-Linked SEDT
X-Linked Spondyloepiphyseal Dysplasia Tarda
Hyperostosis Corticalis Generalisata - Mais específico
Identificador do conceito M0015522
Termo preferido Hyperostosis Corticalis Generalisata
Termo(s) alternativo(s) Endosteal Hyperostosis, Autosomal Recessive
Hyperphosphatasemia Tarda
Sost Sclerosing Bone Dysplasia
Sost-Related Sclerosing Bone Dysplasia
Van Buchem Disease
Dyschondroplasias - Mais amplo
Identificador do conceito M0015521
Termo preferido Dyschondroplasias
Termo(s) alternativo(s) Dyschondroplasia
Schwartz-Jampel Syndrome, Type 1 - Mais específico
Identificador do conceito M000644441
Termo preferido Schwartz-Jampel Syndrome, Type 1
Termo(s) alternativo(s) Schwartz Jampel Syndrome, Type 1



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