 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.
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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2017 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Osteochondrodysplasias" by people in Profiles.
-
Kemp JP, Morris JA, Medina-Gomez C, Forgetta V, Warrington NM, Youlten SE, Zheng J, Gregson CL, Grundberg E, Trajanoska K, Logan JG, Pollard AS, Sparkes PC, Ghirardello EJ, Allen R, Leitch VD, Butterfield NC, Komla-Ebri D, Adoum AT, Curry KF, White JK, Kussy F, Greenlaw KM, Xu C, Harvey NC, Cooper C, Adams DJ, Greenwood CMT, Maurano MT, Kaptoge S, Rivadeneira F, Tobias JH, Croucher PI, Ackert-Bicknell CL, Bassett JHD, Williams GR, Richards JB, Evans DM. Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis. Nat Genet. 2017 Oct; 49(10):1468-1475.
-
Nampoothiri S, Fern?ndez-Rebollo E, Yesodharan D, Gardella TJ, Rush ET, Langman CB, J?ppner H. Jansen Metaphyseal Chondrodysplasia due to Heterozygous H223R-PTH1R Mutations With or Without Overt Hypercalcemia. J Clin Endocrinol Metab. 2016 11; 101(11):4283-4289.
-
Brown WW, J?ppner H, Langman CB, Price H, Farrow EG, White KE, McCormick KL. Hypophosphatemia with elevations in serum fibroblast growth factor 23 in a child with Jansen's metaphyseal chondrodysplasia. J Clin Endocrinol Metab. 2009 Jan; 94(1):17-20.
-
Lantos J. Seeking justice for Priscilla. Camb Q Healthc Ethics. 1996; 5(4):485-92.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|