Papillary craniopharyngioma

disease
On this page

Also known as craniopharyngioma, papillarycraniopharyngioma, papillary (morphologic abnormality)papillary craniopharyngioma (morphologic abnormality)papillary neoplasm of Rathke's pouchpapillary Rathke pouch neoplasmpapillary Rathke's pouch neoplasmpapillary Rathke's pouch tumorpapillary Rathke's pouch tumourpapillary tumor of Rathke's pouchpapillary tumour of Rathke's pouch

Summary

Papillary craniopharyngioma (MONDO:0002788) is a disease and 1 clinical trial. Top therapeutic interventions include cobimetinib and vemurafenib. A subtype of craniopharyngioma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 1

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namepapillary craniopharyngioma
Mondo IDMONDO:0002788
DOIDDOID:3847
NCITC4725
UMLSC0431128
MedGen98125
GARD0023246
Is cancer (heuristic)no

Also known as: craniopharyngioma, papillary · craniopharyngioma, papillary (morphologic abnormality) · papillary craniopharyngioma (morphologic abnormality) · papillary neoplasm of Rathke’s pouch · papillary Rathke pouch neoplasm · papillary Rathke’s pouch neoplasm · papillary Rathke’s pouch tumor · papillary Rathke’s pouch tumour · papillary tumor of Rathke’s pouch · papillary tumour of Rathke’s pouch

Data availability: 1 cell line.

Disease family

This is a subtype of craniopharyngioma. 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 › human disease › disease by etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmbenign neoplasmnervous system benign neoplasmcentral nervous system organ benign neoplasmcraniopharyngiomapapillary craniopharyngioma

Related subtypes (1): adamantinous craniopharyngioma

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
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03224767PHASE2ACTIVE_NOT_RECRUITINGVemurafenib and Cobimetinib in Treating Patients With BRAF V600E Mutation Positive Craniopharyngioma

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
COBIMETINIB41
VEMURAFENIB41
CHEMBL341555301
CHEMBL420955501
CHEMBL453842501
PLX-472001