| Descriptor in English: | Agenesis of Corpus Callosum |
| Descriptor in Spanish: | Agenesia del Cuerpo Calloso |
| Descriptor in Portuguese: | Agenesia do Corpo Caloso |
| Descriptor in 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 |
| 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 |
| History Note: | 2012; for Absence of Corpus Callosum use Acrocallosal Syndrome 2009-2011; for Agenesis of Corpus Callosum use Aicardi Syndrome 2011 |
| DeCS UI: | 54514 |
| Descriptor UI: | D061085 |
| Date Established: | 2012/01/01 |
| Date of Entry: | 2011/06/27 |
| Revision Date: | 2012/07/03 |
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Agenesis of Corpus Callosum
- Preferred
Corpus Callosum Malformation
- Related but not broader or narrower
| 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 |
| Concept UI |
M0556461 |
| Preferred term | Corpus Callosum Malformation |
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