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Descriptor English: Osteochondrodysplasias
Descriptor Spanish: Osteocondrodisplasias
Descriptor Portuguese: Osteocondrodisplasias
Descriptor French: Ostéochondrodysplasies
Entry term(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
Tree number(s): C05.116.099.708
C16.320.728
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D010009
Scope note: Abnormal development of cartilage and bone.
Allowable Qualifiers: 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
Previous Indexing: Bone Diseases (1966-1969)
Bone Diseases, Developmental (1970-1984)
Public MeSH Note: 85; DYSCHONDRODYSPLASIAS was heading DYSCHONDROPLASIA 1963-84; SPONDYLEPIPHYSEAL DYSPLASIA was see MUCOPOLYSACCHARIDOSIS 4 1980-84, was see ECCENTROOSTEOCHONDRODYSPLASIA 1968-79
Online Note: use OSTECHONDRODYSPLASIAS to search DYSCHONDROPLASIAS 1966-84; use MUCOPOLYSACCHARIDOSIS 4 to search SPONDYLOEPIPHYSEAL DYSPLASIA 1968-84
History Note: 85; DYSCHONDRODYSPLASIAS was heading DYSCHONDROPLASIA 1963-84; SPONDYLOEPIPHYSEAL DYSPLASIA was see MUCOPOLYSACCHARIDOSIS 4 1980-84, was see ECCENTROOSTEOCHONDRODYSPLASIA 1968-79
DeCS ID: 10187
Unique ID: D010009
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1985/01/01
Date of Entry: 1984/04/06
Revision Date: 2018/10/10
Osteochondrodysplasias - Preferred
Concept UI M0015525
Scope note Abnormal development of cartilage and bone.
Preferred term Osteochondrodysplasias
Entry term(s) Osteochondrodysplasia
Melnick-Needles Syndrome - Narrower
Concept UI M0015523
Preferred term Melnick-Needles Syndrome
Entry term(s) Melnick Needles Osteodysplasty
Melnick Needles Syndrome
Melnick-Needles Osteodysplasty
Osteodysplasty of Melnick and Needles
Osteodysplasty, Melnick-Needles
Multiple Epiphyseal Dysplasia - Related but not broader or narrower
Concept UI M0015524
Preferred term Multiple Epiphyseal Dysplasia
Myotonic Chondrodystrophy - Related but not broader or narrower
Concept UI M0533083
Preferred term Myotonic Chondrodystrophy
Entry term(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 - Narrower
Concept UI M0015527
Preferred term Spondyloepiphyseal Dysplasia
Entry term(s) Dysplasia, Spondyloepiphyseal
Spondyloepiphyseal Dysplasia Tarda, X-Linked - Narrower
Concept UI M0562747
Preferred term Spondyloepiphyseal Dysplasia Tarda, X-Linked
Entry term(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 - Narrower
Concept UI M0015522
Preferred term Hyperostosis Corticalis Generalisata
Entry term(s) Endosteal Hyperostosis, Autosomal Recessive
Hyperphosphatasemia Tarda
Sost Sclerosing Bone Dysplasia
Sost-Related Sclerosing Bone Dysplasia
Van Buchem Disease
Dyschondroplasias - Broader
Concept UI M0015521
Preferred term Dyschondroplasias
Entry term(s) Dyschondroplasia
Schwartz-Jampel Syndrome, Type 1 - Narrower
Concept UI M000644441
Preferred term Schwartz-Jampel Syndrome, Type 1
Entry term(s) Schwartz Jampel Syndrome, Type 1



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