Human Phenotype Ontology 
Grandparent Node:
expandPrimitive neuroectodermal tumor (HP:0030065)help
Parent Node:
expandCentral primitive neuroectodermal tumor (HP:0030070)help
..Starting node
..expandEpendymoblastoma (HP:0030066)help
Term ID: 30066
Name: Ependymoblastoma
Synonym:
Definition: A highly malignant embryonal tumor of infancy and young childhood characterized by neuroectodermal elements organized in distinctive multilayered rosettes. Ependymoblastomas are large lesions that occur in the supratentorial compartment, typically displaying a physical connection to the ventricular system.
Comments:
Reference: HP:0030066
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMedulloepithelioma (HP:0030071) 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:0030066HP:0030066Ependymoblastoma0 CL E G H


Genes (0) :

Diseases (0) :
 

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