chromosome 17, trisomy 17p

Preferred Label : chromosome 17, trisomy 17p;

MeSH synonym : duplication 17p; trisomy 17p;

Origin ID

C538048;

UMLS CUI

C0795865;

CISMeF manual mappings
- Trisomy 17p (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- 17p duplication [ICD-11 More detail]
- Trisomy 17p [ORDO Disease]
MeSH term(s) associated for indexing
- chromosomes, human, pair 17 [MeSH Descriptor]
- trisomy [MeSH Descriptor]
Record concept(s)
- Chromosome 17, trisomy 17p [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 17p duplication [ICD-11 More detail]
- Trisomy 17p [ORDO Disease]
- Trisomy 17p (disorder) [SNOMED CT concept]