Recurrent Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted

Preferred Label : Recurrent Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted;

NCIt definition : The reemergence of oligodendroglioma, IDH-mutant and 1p/19q-codeleted after a period of remission.;

Neoplastic status : Undetermined;

NCI Metathesaurus CUI : CL1792774;

Details

Origin ID

C188126;

UMLS CUI

C5707602;

Disease may have findings
- Cystic Change [NCIt concept]
- Hemorrhage [NCIt concept]
- Mucoid Stroma Formation [NCIt concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Has cytogenetic abnormalities
- 1p/19q Codeletion [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_excludes_finding
- Anaplastic Lesion [NCIt concept]
- Extensive Necrosis [NCIt concept]
- High Mitotic Activity [NCIt concept]
- Precise Histogenesis Unknown [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Glial Cell [NCIt concept]
- Neoplastic Neuroepithelial Cell [NCIt concept]
- Neoplastic Neuroepithelial Cell and Neoplastic Perineural Cell [NCIt concept]
- Neoplastic Oligodendrocyte [NCIt concept]
disease_has_finding
- Diffuse Pattern [NCIt concept]
- Honeycomb Pattern [NCIt concept]
- Microcalcification [NCIt concept]
- Monomorphic Cellular Infiltrate [NCIt concept]
- Oligodendroglial Component Present [NCIt concept]
- Recurrent Disease [NCIt concept]
disease_has_grade
- Grade 2 [NCIt concept]
- Low Grade [NCIt concept]
disease_has_molecular_abnormality
- IDH Gene Family Mutation [NCIt concept]
disease_has_normal_cell_origin
- Glial Cell [NCIt concept]
- Neuroepithelial Cell [NCIt concept]
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
- Oligodendrocyte [NCIt concept]
disease_has_normal_tissue_origin
- Nerve Tissue, Neuroepithelial Tissue, and Nerve Sheaths [NCIt concept]
- Neuroepithelial Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
disease_mapped_to_gene
- IDH Gene Family [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Gain of Chromosome 7 [NCIt concept]
- Loss of Chromosome 11p [NCIt concept]
- Loss of Chromosome 14 [NCIt concept]
- Loss of Chromosome 22q [NCIt concept]
- Loss of Chromosome 6 [NCIt concept]
- Loss of Chromosome 7 [NCIt concept]

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