MeSH Browser

MeSH Heading: Agenesis of Corpus Callosum
Tree Number(s): C10.500.034; C16.131.666.034; C23.300.008
Unique ID: D061085
RDF Unique Identifier: http://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.
Entry Term(s): Absence of Corpus Callosum; Corpus Callosum Agenesis; Corpus Callosum Dysgenesis; Corpus Callosum Hypogenesis; Corpus Callosum Malformation; Corpus Callosum, Agenesis Of
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
Date Established: 2012/01/01
Date of Entry: 2011/06/27
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)

Agenesis of Corpus Callosum MeSH Descriptor Data 2025