"Craniofacial Dysostosis" 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.
Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia.
Descriptor ID |
D003394
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MeSH Number(s) |
C05.116.099.370.231 C05.660.207.231 C16.131.621.207.231
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Concept/Terms |
Craniofacial Dysostosis- Craniofacial Dysostosis
- Craniofacial Dysostosis Syndrome
- Craniofacial Dysostosis Syndromes
- Craniofacial Dysarthrosis
- Craniofacial Dysarthroses
- Dysarthroses, Craniofacial
- Dysarthrosis, Craniofacial
- Dysostosis, Craniofacial
- Craniofacial Dysostoses
- Dysostoses, Craniofacial
Crouzon Disease- Crouzon Disease
- Craniofacial Dysostosis, Type I
- Crouzon Craniofacial Dysostosis
- Craniofacial Dysostosis, Crouzon
- Craniofacial Dysostosis Type 1
- Crouzon's Disease
- Crouzons Disease
- Crouzon Syndrome
|
Below are MeSH descriptors whose meaning is more general than "Craniofacial Dysostosis".
Below are MeSH descriptors whose meaning is more specific than "Craniofacial Dysostosis".
This graph shows the total number of publications written about "Craniofacial Dysostosis" by people in this website by year, and whether "Craniofacial Dysostosis" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2014 | 1 | 0 | 1 |
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Below are the most recent publications written about "Craniofacial Dysostosis" by people in Profiles.
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Beck AE, McMillin MJ, Gildersleeve HI, Shively KM, Tang A, Bamshad MJ. Genotype-phenotype relationships in Freeman-Sheldon syndrome. Am J Med Genet A. 2014 Nov; 164A(11):2808-13.
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Ma W, Lozanoff S. External craniofacial features, body size, and renal morphology in prenatal brachyrrhine mice. Teratology. 1993 Apr; 47(4):321-32.