chromosome 17 deletion

Preferred Label : chromosome 17 deletion;

CISMeF synonym : 17p- syndrome;

MeSH hyponym : Partial Monosomy 17p; Deletion 17p Syndrome; Interstitial deletion 17p; Chromosome 17p Deletion Syndrome;

Is substance : O;

Détails

Origin ID

C538045;

UMLS CUI

C2931713;

Currated CISMeF NLP mapping
- Deletions of chromosome 17 [ICD-11 Subcategory]
- Loss of Chromosome 17 [NCIt concept]
False automatic mappings
- 17p duplication [ICD-11 More detail]
MeSH term(s) associated for indexing
- Smith-Magenis syndrome [MeSH Descriptor]
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 17 [MeSH Descriptor]
Record concept(s)
- 17p- syndrome [MeSH concept]
- Chromosome 17 deletion [MeSH concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
Validated automatic mappings to BTNT
- chromosome 17p deletion syndrome [Disease (Nov.)]

Position du mot-clé dans l'(les) arborescence(s) :

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