complete trisomy 20 syndrome

Preferred Label : complete trisomy 20 syndrome;

Origin ID

D4-02204;

UMLS CUI

C0265479;

Currated CISMeF NLP mapping
- Complete trisomy 20 syndrome (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Whole chromosome trisomy, mosaicism (mitotic nondisjunction) [ICD-10 Sub-category (who)]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Complete trisomy 20 syndrome (disorder) [SNOMED CT concept]
See also inter- (CISMeF)
- Mosaic trisomy 20 syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome 20, trisomy [MeSH concept]
- Complete trisomy 20 syndrome (disorder) [SNOMED CT concept]
- Duplications of chromosome 20 [ICD-11 Subcategory]
- Mosaic trisomy 20 [ORDO Disease]
- Mosaic trisomy 20 syndrome (disorder) [SNOMED CT concept]
- Trisomy 20 [NCIt concept]
- chromosome 20, trisomy [MeSH Supplementary Concept]