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Descriptor English: Acrocephalosyndactylia
Descriptor Spanish: Acrocefalosindactilia
Descriptor acrocefalosindactilia
Entry term(s) síndrome de Apert
síndrome de Pfeiffer
síndrome de Saethre-Chotzen
Scope note: Craneoestenosis caracterizada por acrocefalia y sindactilia. Probablemente ocurre como un rasgo autosómico dominante y generalmente es debida a una nueva mutación. (Dorland, 27th ed)
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
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
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000168
Scope note: Congenital craniostenosis with syndactyly.
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
Related: Receptor, Fibroblast Growth Factor, Type 2 MeSH
Twist-Related Protein 1 MeSH
DeCS ID: 174
Unique ID: D000168
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
Acrocephalosyndactylia - Preferred
Concept UI M0000253
Scope note Congenital craniostenosis with syndactyly.
Preferred term Acrocephalosyndactylia
Entry term(s) Acrocephalosyndactylias
Kurczynski Casperson Syndrome
Syndrome, Kurczynski Casperson
Apert-Crouzon Disease - Narrower
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
Saethre-Chotzen Syndrome - Narrower
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
Apert Syndrome - Narrower
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
Pfeiffer Syndrome - Narrower
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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