t(3;5)(q25;q34)

Preferred Label : t(3;5)(q25;q34);

NCIt synonyms : t 3 5 q25 q34;

NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q25) of chromosome 3 and the long arm (q34) of chromosome 5. It is associated with the development of acute myeloid leukemia arising from myelodysplastic syndrome, acute myeloid leukemia with multilineage dysplasia, and acute myeloid leukemia with myelodysplasia-related changes.;

Détails

Origin ID

C36415;

UMLS CUI

C1515766;

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]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 3 [NCIt concept]
- Human Chromosome 5 [NCIt concept]
is_abnormality_of_gene
- NPM1/MLF1 Fusion Gene [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]
molecular_abnormality_involves_gene
- MLF1 Gene [NCIt concept]
- NPM1 Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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