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Acute Myeloid Leukemia, Kit Exon 17 Mutation (MONDO:0100418)

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.)

Overview

Category

musculoskeletal system disorder

connective tissue disorder

immune system disorder

hematologic disorder

Ontology ID

MONDO:0100418

Internal:24145

Synonyms

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

Mapped terms

GARD:0026201

Child terms

Unknown children.

Results

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