chromosome 22, trisomy - CISMeF

" /> chromosome 22, trisomy - CISMeF

CISMeF

chu

Chromosome 22, trisomyMeSH Supplementary Concept

Preferred Label : chromosome 22, trisomy;

MeSH synonym : trisomy 22; duplication 22;

Details

Origin ID

C536799;

UMLS CUI

C0265490;

Automatic exact mappings (from CISMeF team)
- Other specified trisomies and partial trisomies of autosomes [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Complete trisomy 22 syndrome (disorder) [SNOMED CT concept]
- Trisomy 22 [NCIt concept]
- Trisomy 22 [MedDRA Preferred Term]
- Trisomy 22 (disorder) [SNOMED CT concept]
- complete trisomy 22 syndrome [SNOMED Notion]
MeSH term(s) associated for indexing
- chromosomes, human, pair 22 [MeSH Descriptor]
- trisomy [MeSH Descriptor]
Record concept(s)
- Chromosome 22, trisomy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Complete trisomy 22 syndrome (disorder) [SNOMED CT concept]
- Trisomy 22 [MedDRA Preferred Term]
- Trisomy 22 [NCIt concept]
- Trisomy 22 (disorder) [SNOMED CT concept]
- complete trisomy 22 syndrome [SNOMED Notion]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
16/05/2024

© Rouen University Hospital. Any partial or total use of this material must mention the source.