Osteochondrodysplasias

"Osteochondrodysplasias" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Abnormal development of cartilage and bone.

Descriptor ID	D010009
MeSH Number(s)	C05.116.099.708 C16.320.728
Concept/Terms	Osteochondrodysplasias Osteochondrodysplasias Osteochondrodysplasia Melnick-Needles Syndrome Melnick-Needles Syndrome Melnick Needles Syndrome Osteodysplasty of Melnick and Needles Melnick-Needles Osteodysplasty Melnick Needles Osteodysplasty Osteodysplasty, Melnick-Needles Multiple Epiphyseal Dysplasia Multiple Epiphyseal Dysplasia Myotonic Chondrodystrophy Myotonic Chondrodystrophy Chondrodystrophy, Myotonic Schwartz Jampel Aberfeld syndrome Schwartz-Jampel Syndrome, Type 1 Schwartz Jampel Syndrome, Type 1 Myotonic Myopathy, Dwarfism, Chondrodystrophy, And Ocular And Facial Abnormalities Spondylo-Epimetaphyseal Dysplasia With Myotonia Chondrodystrophic Myotonia Myotonia, Chondrodystrophic SJA Syndrome Schwartz-Jampel Syndrome Schwartz Jampel Syndrome Schwartz-Jampel-Aberfeld Syndrome Syndrome, Schwartz-Jampel-Aberfeld Spondyloepiphyseal Dysplasia Spondyloepiphyseal Dysplasia Dysplasia, Spondyloepiphyseal Spondyloepiphyseal Dysplasia Tarda, X-Linked Spondyloepiphyseal Dysplasia Tarda, X-Linked Spondyloepiphyseal Dysplasia Tarda, X Linked X-Linked Spondyloepiphyseal Dysplasia Tarda X Linked Spondyloepiphyseal Dysplasia Tarda X-Linked SEDT SEDT, X-Linked X Linked SEDT SED Tarda X-Linked SED SED, X-Linked X Linked SED Spondyloepiphyseal Dysplasia, Late Late Spondyloepiphyseal Dysplasia Late-Onset Spondyloepiphyseal Dysplasia Late Onset Spondyloepiphyseal Dysplasia Spondyloepiphyseal Dysplasia, Late-Onset Hyperostosis Corticalis Generalisata Hyperostosis Corticalis Generalisata Sost Sclerosing Bone Dysplasia Van Buchem Disease Sost-Related Sclerosing Bone Dysplasia Endosteal Hyperostosis, Autosomal Recessive Hyperphosphatasemia Tarda Dyschondroplasias Dyschondroplasias Dyschondroplasia

Below are MeSH descriptors whose meaning is more general than "Osteochondrodysplasias".

Diseases [C]
Musculoskeletal Diseases [C05]
Bone Diseases [C05.116]
Bone Diseases, Developmental [C05.116.099]
Osteochondrodysplasias [C05.116.099.708]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Osteochondrodysplasias [C16.320.728]

Below are MeSH descriptors whose meaning is related to "Osteochondrodysplasias".

Below are MeSH descriptors whose meaning is more specific than "Osteochondrodysplasias".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Osteochondrodysplasias" by people in this website by year, and whether "Osteochondrodysplasias" was a major or minor topic of these publications.

Bar chart showing 2 publications over 2 distinct years, with a maximum of 1 publications in 2019 and 2021

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2019	0	1	1
2021	1	0	1

Below are the most recent publications written about "Osteochondrodysplasias" by people in Profiles.

Castellanos BS, Reyes-Nava NG, Quintana AM. Knockdown of hspg2 is associated with abnormal mandibular joint formation and neural crest cell dysfunction in zebrafish. BMC Dev Biol. 2021 03 08; 21(1):7.

View in: PubMed
Buchbinder D, Hauck F, Albert MH, Rack A, Bakhtiar S, Shcherbina A, Deripapa E, Sullivan KE, Perelygina L, Eloit M, Neven B, P?rot P, Moshous D, Suarez F, Bodemer C, Bonilla FA, Vaz LE, Krol AL, Klein C, Seppanen M, Nugent DJ, Singh J, Ochs HD. Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders. J Clin Immunol. 2019 01; 39(1):81-89.

View in: PubMed
Seo SG, Song HR, Kim HW, Yoo WJ, Shim JS, Chung CY, Park MS, Oh CW, Jeong C, Song KS, Kim OH, Park SS, Choi IH, Cho TJ. Comparison of orthopaedic manifestations of multiple epiphyseal dysplasia caused by MATN3 versus COMP mutations: a case control study. BMC Musculoskelet Disord. 2014 Mar 15; 15:84.

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Kim OH, Park H, Seong MW, Cho TJ, Nishimura G, Superti-Furga A, Unger S, Ikegawa S, Choi IH, Song HR, Kim HW, Yoo WJ, Shim JS, Chung CY, Oh CW, Jeong C, Song KS, Seo SG, Cho SI, Yeo IK, Kim SY, Park S, Park SS. Revisit of multiple epiphyseal dysplasia: ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes. Am J Med Genet A. 2011 Nov; 155A(11):2669-80.

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Cho TJ, Choi IH, Chung CY, Yoo WJ, Park MS, Lee DY. Hemiepiphyseal stapling for angular deformity correction around the knee joint in children with multiple epiphyseal dysplasia. J Pediatr Orthop. 2009 Jan-Feb; 29(1):52-6.

View in: PubMed

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