Chromosomal Insertion

Preferred Label : Chromosomal Insertion;

NCIt synonyms : ins;

NCIt definition : A chromosomal rearrangement in which a segment a segment of DNA is added internally to a chromosome.;

Details

Origin ID

C6828;

UMLS CUI

C1516518;

Automatic exact mappings (from CISMeF team)
- Chromosome insertion [PASCAL descriptor]
- Inch/second (qualifier value) [SNOMED CT concept]
False automatic mappings
- Infantile nystagmus syndrome (disorder) [SNOMED CT concept]
- Insulin [OMIM Phenotype]
- insulin [MeSH Descriptor]
- insulin (human) [Substance BNPC]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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