macroencephaly

Preferred Label : macroencephaly;

Origin ID

D4-91500;

UMLS CUI

C2720434;

Automatic exact mappings (from CISMeF team)
- malformations of cortical development [MeSH Descriptor]
Currated CISMeF NLP mapping
- Macroencephaly (disorder) [SNOMED CT concept]
- Megalencephaly [PASCAL descriptor]
- Megalencephaly [MeSH Descriptor]
- Megalencephaly [MeSH concept]
- Megalencephaly [ICD-10 Sub-category]
- Megalencephaly [HPO term]
- Megalencephaly [ICD-11 Subcategory]
- Megalencephaly [ICD-10 Sub-category (who)]
- Megalencephaly [ORDO Disease]
- Megalencephaly [HRDO Sign]
- Megalencephaly, autosomal dominant [OMIM Phenotype]
ICD-10 exact mapping(s)
- Megalencephaly [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Non-syndromic central nervous system malformation [ORDO Disease]
Metaterm(s)
- neurosurgery [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
Référence SNOMED
- congenital hypertrophy, nos [SNOMED Notion]
- head, nos [SNOMED Notion]
SNOMED CT concept
- Macroencephaly (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Macrencephaly [MedDRA LLT]
- Macroencephaly [MedDRA LLT]
- Macroencephaly (disorder) [SNOMED CT concept]
- Megalencephaly [ICD-10 Sub-category]
- Megalencephaly [ORDO Disease]
- Megalencephaly [ICD-10 Sub-category (who)]