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Craniofacial Dysostosis MeSH Descriptor Data 2024


MeSH Heading
Craniofacial Dysostosis
Tree Number(s)
C05.116.099.370.231
C05.660.207.231
C16.131.621.207.231
Unique ID
D003394
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D003394
Annotation
"craniofacial dysmorphism" does not go here: index under FACIAL BONES / abnorm + SKULL / abnorm but not also ABNORMALITIES, MULTIPLE
Scope Note
Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia.
Entry Term(s)
Craniofacial Dysarthrosis
Craniofacial Dysostosis Syndrome
Craniofacial Dysostosis Type 1
Craniofacial Dysostosis, Type I
Crouzon Craniofacial Dysostosis
Crouzon Disease
Crouzon Syndrome
Crouzon's Disease
Dysostosis, Craniofacial
NLM Classification #
WE 705
See Also
Receptor, Fibroblast Growth Factor, Type 2
Date Established
1966/01/01
Date of Entry
1999/01/01
Revision Date
2016/01/19
Craniofacial Dysostosis Preferred
Crouzon Disease Narrower
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