NPM1 Gene Mutation

Preferred Label : NPM1 Gene Mutation;

NCIt synonyms : Mutation of the Nucleophosmin Gene; NPM1 Mutation; Nucleophosmin Gene Mutation;

NCIt definition : Mutation of the nucleophosmin gene. It is seen in acute myeloid leukemias usually associated with a normal karyotype.;

Détails

Origin ID

C82429;

UMLS CUI

C2826175;

Automatic exact mappings (from CISMeF team)
- NPM1 gene mutation [MedDRA Preferred Term]
- Nucleophosmin gene mutation [MedDRA LLT]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- NPM1 gene mutation [MedDRA Preferred Term]
- Nucleophosmin gene mutation [MedDRA LLT]
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]
is_molecular_abnormality_of_disease
- Acute Myeloid Leukemia with NPM1 Mutation [NCIt concept]
molecular_abnormality_involves_gene
- NPM1 Gene [NCIt concept]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients