Pineal parenchymal tumor of intermediate differentiation

disease
On this page

Also known as pineal parenchymal tumor of intermediate differentiation (morphologic abnormality)pineal parenchymal tumors of intermediate differentiationpineal parenchymal tumour of intermediate differentiation (morphologic abnormality)pineal parenchymal tumours of intermediate differentiationPPTID

Summary

Pineal parenchymal tumor of intermediate differentiation (MONDO:0006369) is a cancer and 1 clinical trial. Top therapeutic interventions include filgrastim and sonidegib. 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

FieldValue
Canonical namepineal parenchymal tumor of intermediate differentiation
Mondo IDMONDO:0006369
EFOEFO:1000474
Orphanet251919
DOIDDOID:5030
NCITC6967
SNOMED CT715904005
UMLSC1367859
MedGen234566
GARD0010644
Is cancer (heuristic)yes

Also known as: pineal parenchymal tumor of intermediate differentiation · pineal parenchymal tumor of intermediate differentiation (morphologic abnormality) · pineal parenchymal tumors of intermediate differentiation · pineal parenchymal tumour of intermediate differentiation (morphologic abnormality) · pineal parenchymal tumours of intermediate differentiation · PPTID

Disease family

Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmnervous system neoplasmneuroepithelial neoplasm › pineal parenchymal cell neoplasm › pineal parenchymal tumor of intermediate differentiation

Related subtypes (2): adult pineal parenchymal tumor, pineocytoma

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)

PhaseTrials
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03434262PHASE1COMPLETEDSJDAWN: St. Jude Children’s Research Hospital Phase 1 Study Evaluating Molecularly-Driven Doublet Therapies for Children and Young Adults With Recurrent Brain Tumors

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
FILGRASTIM41
SONIDEGIB41