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Descriptor English: Agenesis of Corpus Callosum
Descriptor Spanish: Agenesia del Cuerpo Calloso
Descriptor agenesia del cuerpo calloso
Entry term(s) ausencia del cuerpo calloso
Scope note: Defecto del nacimiento que puede dar lugar a una ausencia parcial o completa del CUERPO CALLOSO. Puede ser aislado o parte de un síndrome (ej., SÍNDROME DE AICARDI; SÍNDROME ACROCALLOSAL; SÍNDROME DE ANDERMANN; y HOLOPROSENCEFALIA). Las manifestaciones clínicas incluyen deterioro de la destreza neuromotora y DISCAPACIDAD INTELECTUAL de variable severidad.
Descriptor Portuguese: Agenesia do Corpo Caloso
Descriptor French: Agénésie du corps calleux
Entry term(s): Absence of Corpus Callosum
Ageneses, Corpus Callosum
Agenesis, Corpus Callosum
Corpus Callosum Absence
Corpus Callosum Absences
Corpus Callosum Ageneses
Corpus Callosum Agenesis
Corpus Callosum Dysgeneses
Corpus Callosum Dysgenesis
Corpus Callosum Hypogeneses
Corpus Callosum Hypogenesis
Corpus Callosum Malformation
Corpus Callosum, Agenesis Of
Dysgeneses, Corpus Callosum
Dysgenesis, Corpus Callosum
Hypogeneses, Corpus Callosum
Hypogenesis, Corpus Callosum
Tree number(s): C10.500.034
C16.131.666.034
C23.300.008
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D061085
Scope note: Birth defect that results in a partial or complete absence of the CORPUS CALLOSUM. It may be isolated or a part of a syndrome (e.g., AICARDI'S SYNDROME; ACROCALLOSAL SYNDROME; ANDERMANN SYNDROME; and HOLOPROSENCEPHALY). Clinical manifestations include neuromotor skill impairment and INTELLECTUAL DISABILITY of variable severity.
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
Previous Indexing: Corpus Callosum/abnormalities (1971-2011)
Public MeSH Note: 2012; for Absence of Corpus Callosum see Acrocallosal Syndrome 2009-2011; for Agenesis of Corpus Callosum see Aicardi Syndrome 2011
History Note: 2012; for Absence of Corpus Callosum use Acrocallosal Syndrome 2009-2011; for Agenesis of Corpus Callosum use Aicardi Syndrome 2011
DeCS ID: 54514
Unique ID: D061085
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2012/01/01
Date of Entry: 2011/06/27
Revision Date: 2012/07/03
Agenesis of Corpus Callosum - Preferred
Concept UI M0519523
Scope note Birth defect that results in a partial or complete absence of the CORPUS CALLOSUM. It may be isolated or a part of a syndrome (e.g., AICARDI'S SYNDROME; ACROCALLOSAL SYNDROME; ANDERMANN SYNDROME; and HOLOPROSENCEPHALY). Clinical manifestations include neuromotor skill impairment and INTELLECTUAL DISABILITY of variable severity.
Preferred term Agenesis of Corpus Callosum
Entry term(s) Absence of Corpus Callosum
Ageneses, Corpus Callosum
Agenesis, Corpus Callosum
Corpus Callosum Absence
Corpus Callosum Absences
Corpus Callosum Ageneses
Corpus Callosum Agenesis
Corpus Callosum Dysgeneses
Corpus Callosum Dysgenesis
Corpus Callosum Hypogeneses
Corpus Callosum Hypogenesis
Corpus Callosum, Agenesis Of
Dysgeneses, Corpus Callosum
Dysgenesis, Corpus Callosum
Hypogeneses, Corpus Callosum
Hypogenesis, Corpus Callosum
Corpus Callosum Malformation - Related but not broader or narrower
Concept UI M0556461
Preferred term Corpus Callosum Malformation



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