t(7;11)(p15;p15) - CISMeF

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CISMeF

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T(7;11)(p15;p15)NCIt concept

Preferred Label : t(7;11)(p15;p15);

NCIt synonyms : t 7 11 p15 p15;

Details

Origin ID

C36609;

UMLS CUI

C1515783;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 11 [NCIt concept]
- Human Chromosome 7 [NCIt concept]
is_abnormality_of_gene
- NUP98/HOXA9 Fusion Gene [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Acute Myelomonocytic Leukemia without Abnormal Eosinophils [NCIt concept]

Keyword's position in hierarchy(ies) :

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15/05/2024

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