Adult pineal parenchymal tumor
diseaseOn this page
Also known as adult pineal gland neoplasmadult pineal gland tumoradult pineal gland tumouradult pineal parenchymal cell neoplasmadult pineal parenchymal cell tumoradult pineal parenchymal cell tumouradult pineal parenchymal neoplasmparenchymal neoplasm of adult pineal glandparenchymal neoplasm of the adult pineal glandparenchymal tumor of adult pineal glandparenchymal tumor of the adult pineal glandparenchymal tumour of adult pineal glandparenchymal tumour of the adult pineal glandpineal parenchymal cell neoplasm of adultspineal parenchymal cell tumorpineal parenchymal cell tumour
Summary
Adult pineal parenchymal tumor (MONDO:0003248) is a cancer and 1 clinical trial. A subtype of pineal parenchymal cell neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
- Clinical trials: 1
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | adult pineal parenchymal tumor |
| Mondo ID | MONDO:0003248 |
| DOID | DOID:5031 |
| NCIT | C8273 |
| UMLS | C0280794 |
| MedGen | 83710 |
| Is cancer (heuristic) | yes |
Also known as: adult pineal gland neoplasm · adult pineal gland tumor · adult pineal gland tumour · adult pineal parenchymal cell neoplasm · adult pineal parenchymal cell tumor · adult pineal parenchymal cell tumour · adult pineal parenchymal neoplasm · adult pineal parenchymal tumor · parenchymal neoplasm of adult pineal gland · parenchymal neoplasm of the adult pineal gland · parenchymal tumor of adult pineal gland · parenchymal tumor of the adult pineal gland · parenchymal tumour of adult pineal gland · parenchymal tumour of the adult pineal gland · pineal parenchymal cell neoplasm of adults · pineal parenchymal cell tumor · pineal parenchymal cell tumour
Disease family
An umbrella term covering 1 Mondo subtype.
Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › nervous system neoplasm › neuroepithelial neoplasm › pineal parenchymal cell neoplasm › adult pineal parenchymal tumor
Related subtypes (2): pineal parenchymal tumor of intermediate differentiation, pineocytoma
Subtypes (1): adult pineoblastoma
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: 1.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00019578 | PHASE1 | COMPLETED | Stereotactic Radiosurgery in Treating Patients With Brain Tumors |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.