Homozygous CDKN2B Gene Deletion

Preferred Label : Homozygous CDKN2B Gene Deletion;

NCIt synonyms : Homozygous Cyclin Dependent Kinase Inhibitor 2B Gene Deletion; Homozygous MTS2 Gene Deletion; Biallelic CDKN2B Gene Deletion; Biallelic CDKN2B Deletion; Homozygous INK4B Gene Deletion; Homozygous P15 Gene Deletion; Homozygous Cyclin-Dependent Kinase Inhibitor 2B Gene Deletion; Homozygous CDK4I Gene Deletion; Homozygous CDKN2B Deletion; Homozygous p15INK4b Gene Deletion; Homozygous TP15 Gene Deletion;

NCIt definition : A molecular abnormality referring to the loss of both copies of the CDKN2B gene.;

NCI Metathesaurus CUI : CL1773407;

Details

Origin ID

C185173;

UMLS CUI

C5575937;

Molecular abnormality of diseases
- Astrocytoma, IDH-Mutant, Grade 4 [NCIt concept]
- Childhood Pleomorphic Xanthoastrocytoma [NCIt concept]
- Pleomorphic Xanthoastrocytoma [NCIt concept]
- Recurrent Astrocytoma, IDH-Mutant, Grade 4 [NCIt concept]
- Recurrent Childhood Pleomorphic Xanthoastrocytoma [NCIt concept]
- Supratentorial Pleomorphic Xanthoastrocytoma [NCIt concept]
- Temporal Lobe Pleomorphic Xanthoastrocytoma [NCIt concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 9 [NCIt concept]
molecular_abnormality_involves_gene
- CDKN2B Gene [NCIt concept]

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