t(17;21)(q11;q22) - CISMeF

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CISMeF

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T(17;21)(q11;q22)NCIt concept

Preferred Label : t(17;21)(q11;q22);

NCIt synonyms : t 17 21 q11 q22;

Details

Origin ID

C36615;

UMLS CUI

C1515730;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 17 [NCIt concept]
- Human Chromosome 21 [NCIt concept]

Keyword's position in hierarchy(ies) :

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31/05/2025

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