Thalamic cancer
diseaseOn this page
Also known as cancer of dorsal plus ventral thalamusdorsal plus ventral thalamus cancermalignant dorsal plus ventral thalamus neoplasmmalignant neoplasm of dorsal plus ventral thalamusmalignant neoplasm of thalamusmalignant neoplasm of the thalamusmalignant thalamic neoplasmmalignant thalamic neoplasmsmalignant thalamic tumormalignant thalamic tumorsmalignant thalamic tumourmalignant thalamic tumoursmalignant thalamus neoplasmmalignant thalamus neoplasmsmalignant thalamus tumormalignant thalamus tumorsmalignant thalamus tumourmalignant thalamus tumoursmalignant tumor of thalamusmalignant tumor of the thalamus
Summary
Thalamic cancer (MONDO:0003766) is a cancer. A subtype of diencephalic cancer — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | thalamic cancer |
| Mondo ID | MONDO:0003766 |
| DOID | DOID:6098 |
| ICD-11 | 610018988 |
| NCIT | C4576 |
| SNOMED CT | 188287005 |
| UMLS | C0346902 |
| MedGen | 83429 |
| GARD | 0027647 |
| Anatomy (UBERON) | UBERON:0001897 |
| Is cancer (heuristic) | yes |
Also known as: cancer of dorsal plus ventral thalamus · dorsal plus ventral thalamus cancer · malignant dorsal plus ventral thalamus neoplasm · malignant neoplasm of dorsal plus ventral thalamus · malignant neoplasm of thalamus · malignant neoplasm of the thalamus · malignant thalamic neoplasm · malignant thalamic neoplasms · malignant thalamic tumor · malignant thalamic tumors · malignant thalamic tumour · malignant thalamic tumours · malignant thalamus neoplasm · malignant thalamus neoplasms · malignant thalamus tumor · malignant thalamus tumors · malignant thalamus tumour · malignant thalamus tumours · malignant tumor of thalamus · malignant tumor of the thalamus (+3 more)
Disease family
This is a subtype of diencephalic cancer. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › nervous system cancer › central nervous system cancer › brain cancer › supratentorial cancer › diencephalic cancer › thalamic cancer
Related subtypes (2): diencephalic astrocytomas, chordoid glioma of the third ventricle
Subtypes (2): pituitary cancer, pineal gland cancer
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 0.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.