Microgyria - CISMeF

Preferred Label : Microgyria;

NCIt definition : A congenital abnormality characterized by the presence of abnormally small convolutions in the brain. It results in mental retardation.;

Details

Origin ID

C98988;

UMLS CUI

C2362742;

Automatic exact mappings (from CISMeF team)
- Other reduction deformities of brain [ICD-10 Sub-category (who)]
- Other reduction deformities of brain [ICD-10 Sub-category]
Currated CISMeF NLP mapping
- Microgyria (disorder) [SNOMED CT concept]
- Polymicrogyria [MedDRA Preferred Term]
- Polymicrogyria [ORDO Disease]
- Polymicrogyria [PASCAL descriptor]
- Polymicrogyria [MeSH Descriptor]
- Polymicrogyria [HPO term]
- microgyria [SNOMED Notion]
- polymicrogyria [Disease (Nov.)]
- polymicrogyria [Radlex concept]
- polymicrogyria [MeSH concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Microgyria (disorder) [SNOMED CT concept]
- microgyria [SNOMED Notion]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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