Congenital malformations of corpus callosum

Preferred Label : Congenital malformations of corpus callosum;

Inclusion CIM-10 : Agenesis of corpus callosum;

Diag associé à un acte (%) : 75.3;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q040;

UMLS CUI

C0431366;

Automatic exact mappings (from CISMeF team)
- Agenesis of corpus callosum [HPO term]
- Agenesis of corpus callosum (disorder) [SNOMED CT concept]
- Congenital malformation of corpus callosum (disorder) [SNOMED CT concept]
- Corpus callosum agenesis [ICD-11 Subcategory]
- Corpus callosum agenesis [MedDRA LLT]
- Corpus callosum agenesis [PASCAL descriptor]
- Corpus callosum, agenesis of [OMIM Phenotype]
- agenesis of corpus callosum [MeSH Descriptor]
- agenesis of corpus callosum [MeSH concept]
Excluded by
- Other reduction deformities of brain [ICD-10 Sub-category]
Orphanet concepts
- Acrocallosal syndrome [ORDO Disease]
- Aicardi syndrome [ORDO Disease]
- Corpus callosum agenesis-macrocephaly-hypertelorism syndrome [ORDO Disease]
- Isolated corpus callosum agenesis [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital malformation of corpus callosum (disorder) [SNOMED CT concept]
- Corpus callosum agenesis [ICD-11 Subcategory]
Validated automatic mappings to BTNT
- Corpus Callosum Agenesis [NCIt concept]

Keyword's position in hierarchy(ies) :

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