Monoallelic Mutation

Preferred Label : Monoallelic Mutation;

NCIt definition : A mutation that occurs on one allele of a gene.;

NCI Metathesaurus CUI : CL512982;

Details

Origin ID

C129830;

UMLS CUI

C4330703;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
is_molecular_abnormality_of_disease
- Acute Myeloid Leukemia with Monoallelic CEBPA Mutation [NCIt concept]
- Hematologic Neoplasm with Germline RUNX1 Mutation [NCIt concept]

Keyword's position in hierarchy(ies) :

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