Monosomy 5 - CISMeF

Preferred Label : Monosomy 5;

NCIt definition : A cytogenetic aneuploidy abnormality that refers to the presence of one chromosome 5 only. It is associated with the development of refractory anemia with excess blasts, refractory anemia with multilineage dysplasia, and refractory anemia with multilineage dysplasia and ringed sideroblasts.;

Details

Origin ID

C36523;

UMLS CUI

C1513481;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- AML Authorized Value Terminology [NCIt concept]
- AML Minimal Residual Disease Table [NCIt concept]
- AML Molecular Analysis Table [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 5 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Childhood Myelodysplastic Syndrome with Excess Blasts [NCIt concept]
- Myelodysplastic Syndrome with Excess Blasts [NCIt concept]
- Myelodysplastic Syndrome with Excess Blasts and Fibrosis [NCIt concept]
- Myelodysplastic Syndrome with Excess Blasts-1 [NCIt concept]
- Myelodysplastic Syndrome, Not Otherwise Specified with Multilineage Dysplasia [NCIt concept]
- Myelodysplastic Syndrome/Acute Myeloid Leukemia [NCIt concept]

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