Human Phenotype Ontology 
Grandparent Node:
Abnormality of the pancreas (HP:0001732)help
Grandparent Node:
Neoplasm by anatomical site (HP:0011793)help
Parent Node:
Neoplasm of the pancreas (HP:0002894)help
..Starting node
Pancreatoblastoma (HP:0100757)help
Term ID: 100757
Name: Pancreatoblastoma
Definition: A rare pediatric carcinoma of the pancreas.
Reference: HP:0100757
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandPancreatic adenocarcinoma (HP:0006725) help
..expandPancreatic islet cell adenoma (HP:0008261) help
..expandPancreatic squamous cell carcinoma (HP:0012142) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100757HP:0100757Pancreatoblastoma0BRD4 CL E G H2347613575ORPHA:443167NUT midline carcinomaHP:0040282 - Frequent
HP:0100757HP:0100757Pancreatoblastoma0NUTM1 CL E G H25664629919ORPHA:443167NUT midline carcinomaHP:0040282 - Frequent

Genes (2) :BRD4 NUTM1

Diseases (1) :ORPHA:443167

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.