"Bone Diseases, Developmental" 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.
Diseases resulting in abnormal GROWTH or abnormal MORPHOGENESIS of BONES.
| Descriptor ID |
D001848
|
| MeSH Number(s) |
C05.116.099
|
| Concept/Terms |
Bone Diseases, Developmental- Bone Diseases, Developmental
- Bone Dysplasias
- Bone Dysplasia
- Dysplasia, Bone
- Dysplasias, Bone
- Developmental Bone Disease
- Bone Disease, Developmental
- Developmental Bone Diseases
|
Below are MeSH descriptors whose meaning is more general than "Bone Diseases, Developmental".
Below are MeSH descriptors whose meaning is more specific than "Bone Diseases, Developmental".
This graph shows the total number of publications written about "Bone Diseases, Developmental" by people in this website by year, and whether "Bone Diseases, Developmental" 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 |
|---|
| 2002 | 1 | 0 | 1 |
| 2012 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Bone Diseases, Developmental" by people in Profiles.
-
ANKRD11 variants: KBG syndrome and beyond. Clin Genet. 2021 08; 100(2):187-200.
-
Post-weaning epiphysiolysis causes distal femur dysplasia and foreshortened hindlimbs in fetuin-A-deficient mice. PLoS One. 2017; 12(10):e0187030.
-
Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3. Hum Genet. 2015 Jul; 134(7):691-704.
-
Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly. Eur J Hum Genet. 2012 Jun; 20(6):705-8.
-
Microlissencephaly in microcephalic osteodysplastic primordial dwarfism: a case report and review of the literature. Neuropediatrics. 2002 Dec; 33(6):309-13.
MeSH information
