RARA Gene Rearrangement

Preferred Label : RARA Gene Rearrangement;

NCIt synonyms : Retinoic Acid Receptor Alpha Gene Rearrangement; NR1B1 Gene Rearrangement; RARalpha Gene Rearrangement; RARA Rearrangement;

NCIt definition : A molecular abnormality indicating rearrangement of the RARA gene.;

Details

Origin ID

C186964;

UMLS CUI

C4068344;

Automatic exact mappings (from CISMeF team)
- RARA gene rearrangements [LOINC component]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- RARA gene rearrangements [LOINC component]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 17 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with BCOR-RARA [NCIt concept]
- Acute Myeloid Leukemia with FIP1L1-RARA [NCIt concept]
- Acute Myeloid Leukemia with STAT3-RARA [NCIt concept]
- Acute Myeloid Leukemia with STAT5B-RARA [NCIt concept]
- Acute Myeloid Leukemia with TBL1XR1-RARA [NCIt concept]
- Acute Myeloid Leukemia with a Variant RARA Rearrangement [NCIt concept]
- Acute Myeloid Leukemia with t(11;17)(q13;q21); NUMA1-RARA [NCIt concept]
- Acute Myeloid Leukemia with t(11;17)(q23;q21); ZBTB16-RARA [NCIt concept]
- Acute Myeloid Leukemia with t(1;17)(q42.3;q21.2); IRF2BP2-RARA [NCIt concept]
- Acute Myeloid Leukemia with t(5;17)(q35;q21); NPM1-RARA [NCIt concept]
- Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA [NCIt concept]
- Adult Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA [NCIt concept]
- Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA [NCIt concept]
- Microgranular Acute Promyelocytic Leukemia [NCIt concept]
- Recurrent Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA [NCIt concept]
- Typical Acute Promyelocytic Leukemia [NCIt concept]
molecular_abnormality_involves_gene
- RARA Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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