t(1;3)(p36;q23-25)

Preferred Label : t(1;3)(p36;q23-25);

NCIt synonyms : t 1 3 p36 3 q25;

NCIt definition : A cytogenetic abnormality that refers to the translocation of the short arm (p36) of chromosome 1 and the long arm (q23-25) of chromosome 3. It is associated with WWTR1/CAMTA1 fusions.;

Details

Origin ID

C36563;

UMLS CUI

C4053815;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome 3 [NCIt concept]
is_abnormality_of_gene
- WWTR1/CAMTA1 Fusion Gene [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Adult Epithelioid Hemangioendothelioma [NCIt concept]
- Bone Epithelioid Hemangioendothelioma [NCIt concept]
- Cardiac Epithelioid Hemangioendothelioma [NCIt concept]
- Central Nervous System Epithelioid Hemangioendothelioma [NCIt concept]
- Childhood Epithelioid Hemangioendothelioma [NCIt concept]
- Epithelioid Hemangioendothelioma [NCIt concept]
- Epithelioid Hemangioendothelioma with WWTR1-CAMTA1 Gene Fusion [NCIt concept]
- Liver Epithelioid Hemangioendothelioma [NCIt concept]
- Locally Advanced Epithelioid Hemangioendothelioma [NCIt concept]
- Lung Epithelioid Hemangioendothelioma [NCIt concept]
- Mediastinal Epithelioid Hemangioendothelioma [NCIt concept]
- Metastatic Epithelioid Hemangioendothelioma [NCIt concept]
- Pleural Epithelioid Hemangioendothelioma [NCIt concept]
- Sinonasal Epithelioid Hemangioendothelioma [NCIt concept]
molecular_abnormality_involves_gene
- CAMTA1 Gene [NCIt concept]
- WWTR1 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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