RUNX1 Gene Mutation

Preferred Label : RUNX1 Gene Mutation;

NCIt synonyms : AML1 Mutation; CBFalpha2 Mutation; AMLCR1 Gene Mutation; Runt-Related Transcription Factor 1 Gene Mutation; Acute Myeloid Leukemia 1 Gene Mutation; AML1 Gene Mutation; CBFA2 Gene Mutation;

NCIt related terms : RUNX1 Mutation; RUNX1;

NCIt definition : A change in the nucleotide sequence of the RUNX1 gene.;

Details

Origin ID

C38362;

UMLS CUI

C1515852;

Automatic exact mappings (from CISMeF team)
- AML1 gene mutation [MedDRA LLT]
- RUNX family transcription factor 1 [ORDO Gene]
- RUNX1 gene mutation [MedDRA Preferred Term]
- Runt-related transcription factor 1 [OMIM gene]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- AML1 gene mutation [MedDRA LLT]
- RUNX1 gene mutation [MedDRA Preferred Term]
concept_is_in_subset
- AML Authorized Value Terminology [NCIt concept]
- AML Minimal Residual Disease Table [NCIt concept]
- AML Molecular Analysis Table [NCIt concept]
- CPTAC Acute Myeloid Leukemia Baseline Form [NCIt concept]
- CPTAC Baseline Medical Forms Terminology [NCIt concept]
- CPTAC Terminology [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
is_molecular_abnormality_of_disease
- Acute Myeloid Leukemia with RUNX1 Mutation [NCIt concept]
molecular_abnormality_involves_gene
- RUNX1 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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