Homozygous CDKN2A Gene Deletion

Preferred Label : Homozygous CDKN2A Gene Deletion;

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

NCIt definition : A molecular abnormality referring to the loss of both copies of the CDKN2A gene.;

NCI Metathesaurus CUI : CL1773406;

Details

Origin ID

C185171;

UMLS CUI

C5575936;

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]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 9 [NCIt concept]
is_not_molecular_abnormality_of_disease
- Diffuse Low Grade Glioma, BRAF p.V600E-Mutant [NCIt concept]
- Diffuse Low Grade Glioma, FGFR1 Tyrosine Kinase Domain-Duplicated [NCIt concept]
- Diffuse Low Grade Glioma, FGFR1-Mutant [NCIt concept]
- Diffuse Low Grade Glioma, MAPK Pathway-Altered [NCIt concept]
molecular_abnormality_involves_gene
- CDKN2A Gene [NCIt concept]

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