Astrocytoma, IDH-Mutant

Preferred Label : Astrocytoma, IDH-Mutant;

NCIt definition : An astrocytoma associated with IDH1 or IDH2 gene mutations and absence of 1p/19q codeletion. It is classified as grade 2, 3, or 4.;

Neoplastic status : Undetermined;

NCI Metathesaurus CUI : CL1773496;

Details

Origin ID

C185167;

UMLS CUI

C5669733;

Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Grade 4 Lesion [NCIt concept]
- Precise Histogenesis Unknown [NCIt concept]
disease_excludes_molecular_abnormality
- 1p/19q Codeletion [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Astrocyte [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Glial Cell [NCIt concept]
- Neoplastic Neuroepithelial Cell [NCIt concept]
- Neoplastic Neuroepithelial Cell and Neoplastic Perineural Cell [NCIt concept]
disease_has_molecular_abnormality
- IDH Gene Family Mutation [NCIt concept]
disease_has_normal_cell_origin
- Astrocyte [NCIt concept]
- Glial Cell [NCIt concept]
- Neuroepithelial Cell [NCIt concept]
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [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]
pathogenesis_of_disease_involves_gene
- IDH Gene Family [NCIt concept]
- IDH1 Gene [NCIt concept]
- IDH1 wt Allele [NCIt concept]
- IDH2 Gene [NCIt concept]
- IDH2 wt Allele [NCIt concept]

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