congenital cerebral meningocele

Preferred Label : congenital cerebral meningocele;

Origin ID

D4-91042;

UMLS CUI

C0009694;

Currated CISMeF NLP mapping
- Congenital cerebral meningocele (disorder) [SNOMED CT concept]
- Cranial Meningocele [NCIt concept]
- Cranial meningocele [ICD-11 More detail]
- Cranial meningocele [ORDO Disease]
- Meningocele - cerebral (disorder) [SNOMED CT concept]
- Meningocele - cranial (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Encephalocele, unspecified [ICD-10 Sub-category (who)]
Metaterm(s)
- neurosurgery [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
Référence SNOMED
- cerebral meninges, nos [SNOMED Notion]
- congenital failure of fusion with herniated tissue [SNOMED Notion]
- congenital protrusion, nos [SNOMED Notion]
- skull, nos [SNOMED Notion]
SNOMED CT concept
- Congenital cerebral meningocele (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital cerebral meningocele (disorder) [SNOMED CT concept]
- Cranial Meningocele [NCIt concept]
- Cranial meningocele [ORDO Disease]
- Cranial meningocele [ICD-11 More detail]
- Meningocele - cerebral (disorder) [SNOMED CT concept]
- Meningocele - cranial (disorder) [SNOMED CT concept]