| Descriptor English: | Acrocephalosyndactylia | ||||||
| Descriptor Spanish: |
Acrocefalosindactilia
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| Descriptor Portuguese: | Acrocefalossindactilia | ||||||
| Descriptor French: | Acrocéphalosyndactylie | ||||||
| Entry term(s): |
Acrocephalosyndactylias Acrocephalosyndactylies, Type 1 Acrocephalosyndactylies, Type 3 Acrocephalosyndactylies, Type I Acrocephalosyndactylies, Type II Acrocephalosyndactylies, Type III Acrocephalosyndactylies, Type V Acrocephalosyndactyly (Apert) Acrocephalosyndactyly III Acrocephalosyndactyly IIIs Acrocephalosyndactyly, Type 1 Acrocephalosyndactyly, Type 3 Acrocephalosyndactyly, Type I Acrocephalosyndactyly, Type II Acrocephalosyndactyly, Type III Acrocephalosyndactyly, Type V Acrocephaly, Skull Asymmetry, and Mild Syndactyly Apert Crouzon Disease Apert Syndrome Apert-Crouzon Disease Chotzen Syndrome Craniofacial-Skeletal-Dermatologic Dysplasia Disease, Apert-Crouzon Dysostosis Craniofacialis with Hypertelorism Kurczynski Casperson Syndrome Noack Syndrome Noack Syndromes Pfeiffer Syndrome Saethre Chotzen Syndrome Saethre-Chotzen Syndrome Syndactylic Oxycephalies Syndactylic Oxycephaly Syndrome, Apert Syndrome, Chotzen Syndrome, Kurczynski Casperson Syndrome, Noack Syndrome, Pfeiffer Syndrome, Saethre-Chotzen Syndromes, Noack Type I Acrocephalosyndactylies Type I Acrocephalosyndactyly Type II Acrocephalosyndactylies Type II Acrocephalosyndactyly Type III Acrocephalosyndactyly Type V Acrocephalosyndactylies Type V Acrocephalosyndactyly |
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| Tree number(s): |
C05.116.099.370.894.232.015 C05.116.099.370.894.819.100 C05.660.207.240.100 C05.660.585.800.100 C05.660.906.364.100 C05.660.906.819.100 C16.131.621.207.240.100 C16.131.621.585.800.100 C16.131.621.906.364.100 C16.131.621.906.819.100 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000168 | ||||||
| Scope note: | Congenital craniostenosis with syndactyly. |
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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 Twist-Related Protein 1 MeSH | ||||||
| DeCS ID: | 174 | ||||||
| Unique ID: | D000168 | ||||||
| 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: | 2016/07/18 |
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Acrocephalosyndactylia
- Preferred
Apert-Crouzon Disease
- Narrower
Saethre-Chotzen Syndrome
- Narrower
Apert Syndrome
- Narrower
Pfeiffer Syndrome
- Narrower
| Concept UI |
M0000253 |
| Scope note | Congenital craniostenosis with syndactyly. |
| Preferred term | Acrocephalosyndactylia |
| Entry term(s) |
Acrocephalosyndactylias Kurczynski Casperson Syndrome Syndrome, Kurczynski Casperson |
| Concept UI |
M0551744 |
| Preferred term | Apert-Crouzon Disease |
| Entry term(s) |
Acrocephalosyndactylies, Type II Acrocephalosyndactyly, Type II Apert Crouzon Disease Disease, Apert-Crouzon Type II Acrocephalosyndactylies Type II Acrocephalosyndactyly |
| Concept UI |
M0000254 |
| Preferred term | Saethre-Chotzen Syndrome |
| Entry term(s) |
Acrocephalosyndactylies, Type 3 Acrocephalosyndactylies, Type III Acrocephalosyndactyly III Acrocephalosyndactyly IIIs Acrocephalosyndactyly, Type 3 Acrocephalosyndactyly, Type III Acrocephaly, Skull Asymmetry, and Mild Syndactyly Chotzen Syndrome Dysostosis Craniofacialis with Hypertelorism Saethre Chotzen Syndrome Syndrome, Chotzen Syndrome, Saethre-Chotzen Type III Acrocephalosyndactyly |
| Concept UI |
M0000256 |
| Preferred term | Apert Syndrome |
| Entry term(s) |
Acrocephalosyndactylies, Type 1 Acrocephalosyndactylies, Type I Acrocephalosyndactyly (Apert) Acrocephalosyndactyly, Type 1 Acrocephalosyndactyly, Type I Syndactylic Oxycephalies Syndactylic Oxycephaly Syndrome, Apert Type I Acrocephalosyndactylies Type I Acrocephalosyndactyly |
| Concept UI |
M0000255 |
| Preferred term | Pfeiffer Syndrome |
| Entry term(s) |
Acrocephalosyndactylies, Type V Acrocephalosyndactyly, Type V Craniofacial-Skeletal-Dermatologic Dysplasia Noack Syndrome Noack Syndromes Syndrome, Noack Syndrome, Pfeiffer Syndromes, Noack Type V Acrocephalosyndactylies Type V Acrocephalosyndactyly |
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