Aprosencephaly

Preferred Label : Aprosencephaly;

NCIt definition : A very rare congenital brain defect in which the cerebral cortex, striatum, globus pallidus, thalamus, hypothalamus, and eyes are absent or rudimentary.;

Details

Origin ID

C98824;

UMLS CUI

C0431349;

Automatic exact mappings (from CISMeF team)
- Aprosencephaly [ICD-11 More detail]
- Aprosencephaly [ORDO Disease]
- Aprosencephaly syndrome [OMIM Phenotype]
Currated CISMeF NLP mapping
- Aprosencephaly [HPO term]
- Aprosencephaly (disorder) [SNOMED CT concept]
- anencephaly [MeSH Descriptor]
- aprosencephaly [MeSH concept]
See also inter- (CISMeF)
- Anencephaly [ICD-11 Subcategory]
- anencephaly [Disease (Nov.)]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Aprosencephaly [HPO term]
- Aprosencephaly (disorder) [SNOMED CT concept]
- aprosencephaly [MeSH concept]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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