C38392Level 8
KMT2A-ELL Fusion Protein Expression
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A molecular abnormality characterized by the expression of a fusion protein that results from chromosomal recombination involving the human genes KMT2A and ELL. This abnormal protein is associated with acute myeloid leukemia.
**Synonyms:** - MLL-ELL Fusion Protein Expression - MLL/ELL Fusion Protein Expression
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