MeSH Browser

MeSH Heading: Osteochondrodysplasias
Tree Number(s): C05.116.099.708; C16.320.728
Unique ID: D010009
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D010009
Scope Note: Abnormal development of cartilage and bone.
Entry Term(s): Chondrodystrophic Myotonia; Dyschondroplasia; Dyschondroplasias; Endosteal Hyperostosis, Autosomal Recessive; Hyperostosis Corticalis Generalisata; Hyperphosphatasemia Tarda; Late-Onset Spondyloepiphyseal Dysplasia; Melnick-Needles Osteodysplasty; Melnick-Needles Syndrome; Multiple Epiphyseal Dysplasia; Myotonic Chondrodystrophy; Myotonic Myopathy, Dwarfism, Chondrodystrophy, And Ocular And Facial Abnormalities; Osteodysplasty of Melnick and Needles; SED Tarda; SJA Syndrome; Schwartz Jampel Aberfeld syndrome; 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, Late; Van Buchem Disease; X-Linked SED; X-Linked SEDT; X-Linked Spondyloepiphyseal Dysplasia Tarda
NLM Classification #: WE 250
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
Date Established: 1985/01/01
Date of Entry: 1984/04/06
Revision Date: 2018/10/10

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Musculoskeletal Diseases [C05]
- Bone Diseases [C05.116]
  - Bone Diseases, Developmental [C05.116.099]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]

Osteochondrodysplasias Preferred

Hyperostosis Corticalis Generalisata Narrower

Melnick-Needles Syndrome Narrower

Multiple Epiphyseal Dysplasia Related

Spondyloepiphyseal Dysplasia Narrower

Myotonic Chondrodystrophy Related

Spondyloepiphyseal Dysplasia Tarda, X-Linked Narrower

Dyschondroplasias Broader

Schwartz-Jampel Syndrome, Type 1 Narrower

Osteochondrodysplasias MeSH Descriptor Data 2024