Acute myeloid leukemia, KIT exon 17 mutation

Any acute myeloid leukemia that has the chromosomal anomaly KIT exon 17 mutation. (A molecular genetic abnormality indicating the presence of a mutation in exon 17 of the KIT gene located within 4q11-q12.)

Also known as: AML, CD117 Exon 17 Mutation, AML, KIT Proto-Oncogene Tyrosine Protein Kinase Gene Exon 17 Mutation, AML, KIT exon 17 mutation, AML, c-KIT Exon 17 Mutation, AML, v-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog Gene Exon 17 Mutation

3080 clinical trials for this condition and its sub-types, 0 tagged with Acute myeloid leukemia, KIT exon 17 mutation itself.