Aprosencephaly

Preferred Label : Aprosencephaly;

ICD-11 definition : A condition caused by failure of the brain to correctly develop during the antenatal period. This condition is characterized by near total absence of the forebrain with a midline oculofacial defect.;

ICD-11 inclusion : Atelencephaly; Garcia-Lurie syndrome;

Details

Origin ID

1740361952;

Automatic exact mappings (from CISMeF team)
- Aprosencephaly [NCIt concept]
- Aprosencephaly [HPO term]
- Aprosencephaly [ORDO Disease]
- Aprosencephaly (disorder) [SNOMED CT concept]
- anencephaly [MeSH Descriptor]
- aprosencephaly [MeSH concept]
Currated CISMeF NLP mapping
- Aprosencephaly and cerebellar dysgenesis [OMIM Phenotype]
- Aprosencephaly cerebellar dysgenesis [ORDO Disease]
- Aprosencephaly cerebellar dysgenesis (disorder) [SNOMED CT concept]
- aprosencephaly and cerebellar dysgenesis [MeSH Supplementary Concept]
- aprosencephaly and cerebellar dysgenesis [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients