Homozygous CDKN2A Gene Deletion

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A molecular abnormality referring to the loss of both copies of the CDKN2A gene.

**Synonyms:** - Biallelic CDKN2A Deletion - Biallelic CDKN2A Gene Deletion - CDKN2A Gene Null - Homozygous CDK4I Gene Deletion - Homozygous CDKN2A Deletion - Homozygous CDKN2A-p16 Gene Deletion - Homozygous Loss of CDKN2A Gene - Homozygous Loss of Cyclin Dependent Kinase Inhibitor 2A Gene - Homozygous p14ARF Gene Deletion - Homozygous p16 Gene Deletion - Homozygous p16-INK4A Gene Deletion - Homozygous p16INK4a Gene Deletion - Homozygous p19ARF Gene Deletion