del(20q11) - CISMeF

Preferred Label : del(20q11);

NCIt synonyms : del 20 q11; del(20)(q11);

NCIt definition : A cytogenetic abnormality characterized by any loss of genetic material from the long arm of chromosome 20 within the band at 20q11.;

Details

Origin ID

C38386;

UMLS CUI

C1515593;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 20 [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]

Keyword's position in hierarchy(ies) :

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