Encephalocele - CISMeF

Preferred Label : Encephalocele;

ICD-10 exclusion note : Meckel-Gruber syndrome (Q61.9);

Rare : true;

Source : OMS;

Date de début : 01/01/1997;

Date de mise à jour : 01/01/2019;

Do not code with : true;

Details

Origin ID

Q01;

UMLS CUI

C4551722;

Automatic exact mappings (from CISMeF team)
- Congenital cerebral meningocele (disorder) [SNOMED CT concept]
- Encephalocystocele (disorder) [SNOMED CT concept]
- Encephalomyelocele (disorder) [SNOMED CT concept]
- Hydromeningocele - cranial (disorder) [SNOMED CT concept]
- Meningocele - cerebral (disorder) [SNOMED CT concept]
- Meningoencephalocele [HPO term]
- Meningoencephalocele (disorder) [SNOMED CT concept]
- meningocele [MeSH Descriptor]
Currated CISMeF NLP mapping
- Congenital cerebral hernia (disorder) [SNOMED CT concept]
- ENCEPHALOCELE [WHO-ART Preferred Term]
- Encephalocele [NCIt concept]
- Encephalocele [MedDRA Preferred Term]
- Encephalocele [HPO term]
- Encephalocele [ICD-10 category (who)]
- Encephalocele [PASCAL descriptor]
- Encephalocele [ICD-9 code]
- Encephalocele [ICD-11 More detail]
- Encephalocele (disorder) [SNOMED CT concept]
- Isolated encephalocele [ORDO Disease]
- encephalocele [MeSH concept]
- encephalocele [MeSH Descriptor]
- encephalocele [Disease (Nov.)]
- encephalocele, nos [SNOMED Notion]
Excluded by
- Other congenital malformations of skull and face bones [ICD-10 category]
ICD-10 exclusion(s)
- Compression of brain [ICD-10 Sub-category]
- Cystic kidney disease, unspecified [ICD-10 Sub-category]
Metaterm(s)
- neonatology [CISMeF Metaterm]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- ENCEPHALOCELE [WHO-ART Preferred Term]
- Encephalocele [MedDRA Preferred Term]
- Encephalocele [ICD-9 code]
- Encephalocele [HPO term]
- Encephalocele [NCIt concept]
- Encephalocele (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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