Monosomy - CISMeF

Preferred Label : Monosomy;

NCIt definition : A chromosomal abnormality consisting of the absence of one chromosome from the normal diploid number.;

Details

Origin ID

C3239;

UMLS CUI

C0026499;

Currated CISMeF NLP mapping
- Autosomal monosomy [ORDO Disease]
- Monosomy [PASCAL descriptor]
- Monosomy (morphologic abnormality) [SNOMED CT concept]
- monosomy [Disease (Nov.)]
- monosomy [MeSH Descriptor]
- monosomy [MeSH concept]
- monosomy [SNOMED Notion]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal monosomy [ORDO Disease]
- Monosomy [PASCAL descriptor]
- Monosomy (morphologic abnormality) [SNOMED CT concept]
- monosomy [Disease (Nov.)]
- monosomy [MeSH Descriptor]
- monosomy [MeSH concept]
- monosomy [SNOMED Notion]
Validated automatic mappings to BTNT
- Deletions of the autosomes [ICD-11 Category]
concept_is_in_subset
- CPTAC Baseline Medical Forms Terminology [NCIt concept]
- CPTAC Glioblastoma Multiforme Baseline Form [NCIt concept]
- CPTAC Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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