Human Phenotype Ontology 
Grandparent Node:
expandPinealoma (HP:0010799)help
Parent Node:
expandPineal parenchymal cell neoplasm (HP:0030694)help
..Starting node
..expandPineoblastoma (HP:0030408)help
Term ID: 30408
Name: Pineoblastoma
Synonym: Pinealoblastoma
Definition: Pineoblastoma is a rare primitive neuroectodermal tumour (PNET) arising in the pineal gland. Pineoblastomas are classified as a WHO grade IV tumour and comprise one-fourth to one-half of pineal parenchymal tumours. Pineoblastoma is a highly cellular tumor originating in the pineal gland and containing small, poorly differentiated cells.
Comments:
Reference: HP:0030408
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPineocytoma (HP:0030407) 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:0030408HP:0030408Pineoblastoma0 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.