Gain of Chromosome 21

Preferred Label : Gain of Chromosome 21;

NCIt definition : A cytogenetic abnormality that refers to the allelic gain of all or part of chromosome 21.;

Details

Origin ID

C36527;

UMLS CUI

C1517406;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 21 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia Arising from Previous Myelodysplastic Syndrome [NCIt concept]
- Acute Myeloid Leukemia with Multilineage Dysplasia [NCIt concept]
- Acute Myeloid Leukemia, Myelodysplasia-Related [NCIt concept]
- Recurrent Acute Myeloid Leukemia with Multilineage Dysplasia [NCIt concept]
- Recurrent Acute Myeloid Leukemia, Myelodysplasia-Related [NCIt concept]

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