Human Phenotype Ontology 
Grandparent Node:
expand
Morphological central nervous system abnormality (HP:0002011)help
Grandparent Node:
expand
Neoplasm of the nervous system (HP:0004375)help
Parent Node:
expand
Neoplasm of the central nervous system (HP:0100006)help
..Starting node
..expand
Neuronal/glioneuronal neoplasm of the central nervous system (HP:0025170)help
Term ID: 25170
Name: Neuronal/glioneuronal neoplasm of the central nervous system
Synonym: Glioneuronal tumor; Glioneuronal tumour; Neuronal and mixed neuronal-glial tumor; Neuronal and mixed neuronal-glial tumour; Neuronal/glioneuronal neoplasm of the CNS
Definition: A central nervous system neoplasm with neuronal and, less consistently, glial differentiation.
Comments:
Reference: HP:0025170
Genes and Diseases:
 
       Child Nodes:
........expandRosette-forming glioneuronal tumor (HP:0025171) help

 Sister Nodes: 
..expandBenign neoplasm of the central nervous system (HP:0100835) help
..expandBrain neoplasm (HP:0030692) help
..expandMalignant neoplasm of the central nervous system (HP:0100836) help
..expandSpinal cord tumor (HP:0010302) 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:0025170HP:0025170Neuronal/glioneuronal neoplasm of the central nervous system0 CL E G H
HP:0025170HP:0033664Ganglioglioma1 CL E G H
HP:0025170HP:0025171Rosette-forming glioneuronal tumor1 CL E G H
HP:0025170HP:0033703Dysembryoplastic neuroepithelial tumor1 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.