MeSH Browser

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)

Acrocallosal Syndrome MeSH Descriptor Data 2025