"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.
Abnormal development of cartilage and bone.
Descriptor ID |
D010009
|
MeSH Number(s) |
C05.116.099.708 C16.320.728
|
Concept/Terms |
Melnick-Needles Syndrome- Melnick-Needles Syndrome
- Melnick Needles Syndrome
- Osteodysplasty of Melnick and Needles
- Melnick-Needles Osteodysplasty
- Melnick Needles Osteodysplasty
- Osteodysplasty, Melnick-Needles
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 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
|
Below are MeSH descriptors whose meaning is more general than "Osteochondrodysplasias".
Below are MeSH descriptors whose meaning is more specific than "Osteochondrodysplasias".
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.
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Year | Major Topic | Minor Topic | Total |
---|
2015 | 1 | 0 | 1 |
2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Osteochondrodysplasias" by people in Profiles.
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Novel progressive acrodysostosis-like skeletal dysplasia, cerebellar atrophy, and ichthyosis. Am J Med Genet A. 2020 10; 182(10):2214-2221.
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A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred. Clin Genet. 2016 07; 90(1):90-5.