| Descriptor English: | Acrocallosal Syndrome | ||||
| Descriptor Spanish: |
Síndrome Acrocallosal
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| Descriptor Portuguese: | Síndrome Acrocalosal | ||||
| Descriptor French: | Syndrome acrocalleux | ||||
| Entry term(s): |
Acrocallosal Syndromes Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum Syndrome, Acrocallosal Syndromes, Acrocallosal |
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| Tree number(s): |
C10.500.034.500 C16.131.666.034.500 |
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| RDF Unique Identifier: | https://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. |
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| 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 |
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| Previous Indexing: |
Congenital Abnormalities (1963-2008) Corpus Callosum (1963-2008) |
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| Public MeSH Note: | 2009 |
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| History Note: | 2009 |
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| DeCS ID: | 53094 | ||||
| Unique ID: | D055673 | ||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
| Date Established: | 2009/01/01 | ||||
| Date of Entry: | 2008/07/08 | ||||
| Revision Date: | 2012/07/03 |
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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. |
| Preferred term | Acrocallosal Syndrome |
| Entry term(s) |
Acrocallosal Syndromes Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum Syndrome, Acrocallosal Syndromes, Acrocallosal |
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