| Descriptor English: | Craniofacial Dysostosis | ||||||
| Descriptor Spanish: |
Disostosis Craneofacial
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| Descriptor Portuguese: | Disostose Craniofacial | ||||||
| Descriptor French: | Dysostose craniofaciale | ||||||
| Entry term(s): |
Craniofacial Dysarthroses Craniofacial Dysarthrosis Craniofacial Dysostoses Craniofacial Dysostosis Syndrome Craniofacial Dysostosis Syndromes Craniofacial Dysostosis Type 1 Craniofacial Dysostosis, Crouzon Craniofacial Dysostosis, Type I Crouzon Craniofacial Dysostosis Crouzon Disease Crouzon Syndrome Crouzon's Disease Crouzons Disease Dysarthroses, Craniofacial Dysarthrosis, Craniofacial Dysostoses, Craniofacial Dysostosis, Craniofacial |
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| Tree number(s): |
C05.116.099.370.231 C05.660.207.231 C16.131.621.207.231 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D003394 | ||||||
| Scope note: | Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia. |
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| Annotation: | "craniofacial dysmorphism" does not go here: index under FACIAL BONES / abnorm + SKULL / abnorm but not also ABNORMALITIES, MULTIPLE |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Related: |
Receptor, Fibroblast Growth Factor, Type 2
MeSH | ||||||
| DeCS ID: | 3411 | ||||||
| Unique ID: | D003394 | ||||||
| NLM Classification: | WE 705 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1966/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2016/01/19 |
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Craniofacial Dysostosis
- Preferred
Crouzon Disease
- Narrower
| Concept UI |
M0005284 |
| Scope note | Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia. |
| Preferred term | Craniofacial Dysostosis |
| Entry term(s) |
Craniofacial Dysarthroses Craniofacial Dysarthrosis Craniofacial Dysostoses Craniofacial Dysostosis Syndrome Craniofacial Dysostosis Syndromes Dysarthroses, Craniofacial Dysarthrosis, Craniofacial Dysostoses, Craniofacial Dysostosis, Craniofacial |
| Concept UI |
M0554059 |
| Preferred term | Crouzon Disease |
| Entry term(s) |
Craniofacial Dysostosis Type 1 Craniofacial Dysostosis, Crouzon Craniofacial Dysostosis, Type I Crouzon Craniofacial Dysostosis Crouzon Syndrome Crouzon's Disease Crouzons Disease |
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