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Acrocephalosyndactylia MeSH Descriptor Data 2022


MeSH Heading
Acrocephalosyndactylia
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
Unique ID
D000168
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000168
Scope Note
Congenital craniostenosis with syndactyly.
Entry Term(s)
Acrocephalosyndactyly (Apert)
Acrocephalosyndactyly III
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 Syndrome
Apert-Crouzon Disease
Chotzen Syndrome
Craniofacial-Skeletal-Dermatologic Dysplasia
Dysostosis Craniofacialis with Hypertelorism
Kurczynski Casperson Syndrome
Noack Syndrome
Pfeiffer Syndrome
Saethre-Chotzen Syndrome
Syndactylic Oxycephaly
NLM Classification #
WE 705
See Also
Receptor, Fibroblast Growth Factor, Type 2
Twist-Related Protein 1
Date Established
1966/01/01
Date of Entry
1999/01/01
Revision Date
2016/07/18
Acrocephalosyndactylia Preferred
Apert-Crouzon Disease Narrower
Saethre-Chotzen Syndrome Narrower
Apert Syndrome Narrower
Pfeiffer Syndrome Narrower
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