acute myeloid leukemia, monoallelic CEBPA gene mutation

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

Print

Disease Overview

Any acute myeloid leukemia that has the chromosomal anomaly monoallelic CEBPA gene mutation. (The presence of mutations in only one allele of the CEBPA gene.)


Synonyms

  • AML, C/EBP-Alpha Monoallelic Gene Mutation
  • AML, C/EBPalpha Monoallelic Gene Mutation
  • AML, CCAAT Enhancer Binding Protein Alpha Monoallelic Gene Mutation
  • AML, CCAAT/Enhancer Binding Protein Alpha Monoallelic Gene Mutation
  • AML, CCAAT/Enhancer Binding Protein, Alpha Monoallelic Gene Mutation
  • AML, CEBP Monoallelic Gene Mutation
  • AML, CEBPA Monoallelic Gene Mutation
  • AML, CEBPA Monoallelic Mutation
  • AML, moCEBPA
  • AML, monoallelic CEBPA gene mutation

National Organization for Rare Disorders