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Acrocallosal Syndrome
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Acrocallosal Syndrome
Tree Number(s)
C10.500.034.500
C16.131.666.034.500
Unique ID
D055673
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D055673
Scope Note
Autosomal recessive syndrome characterized by hypogenesis or agenesis of
CORPUS CALLOSUM
. Clinical features include
MENTAL RETARDATION
;
CRANIOFACIAL ABNORMALITIES
; digital malformations, and growth retardation.
Entry Term(s)
Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum
Previous Indexing
Congenital Abnormalities (1963-2008)
Corpus Callosum (1963-2008)
Public MeSH Note
2009
History Note
2009
Date Established
2009/01/01
Date of Entry
2008/07/08
Revision Date
2012/07/03
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Nervous System Diseases [C10]
Nervous System Malformations [C10.500]
Agenesis of Corpus Callosum [C10.500.034]
Acrocallosal Syndrome [C10.500.034.500]
Aicardi Syndrome [C10.500.034.687]
Holoprosencephaly [C10.500.034.875]
Septo-Optic Dysplasia [C10.500.034.937]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Nervous System Malformations [C16.131.666]
Agenesis of Corpus Callosum [C16.131.666.034]
Acrocallosal Syndrome [C16.131.666.034.500]
Aicardi Syndrome [C16.131.666.034.687]
Holoprosencephaly [C16.131.666.034.875]
Septo-Optic Dysplasia [C16.131.666.034.937]
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Acrocallosal Syndrome
Preferred
Concept UI
M0519414
Scope Note
Autosomal recessive syndrome characterized by hypogenesis or agenesis of
CORPUS CALLOSUM
. Clinical features include
MENTAL RETARDATION
;
CRANIOFACIAL ABNORMALITIES
; digital malformations, and growth retardation.
Terms
Acrocallosal Syndrome
Preferred Term
Term UI
T716303
Date
03/14/2008
LexicalTag
NON
ThesaurusID
Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum
Term UI
T824600
Date
06/22/2012
LexicalTag
NON
ThesaurusID
OMIM (2013)
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