Human Phenotype Ontology 
Grandparent Node:
expandNervous tissue neoplasm (HP:0030060)help
Parent Node:
expandNeuroectodermal neoplasm (HP:0030061)help
..Starting node
..expandCraniopharyngioma (HP:0030062)help
Term ID: 30062
Name: Craniopharyngioma
Synonym:
Definition: A benign pituitary-region neoplasm that originates from Rathke's pouch. Craniopharyngiomas are benign slow growing tumours that are located within the sellar and para sellar region of the central nervous system.
Comments:
Reference: HP:0030062
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandNeuroepithelial neoplasm (HP:0030063) 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:0030062HP:0030062Craniopharyngioma0H19-ICR CL E G H105259599OMIM:180860Silver-Russell syndrome.
HP:0030062HP:0030062Craniopharyngioma0IGF2 CL E G H34815466OMIM:180860Silver-Russell syndrome.9


Genes (2) :H19-ICR IGF2

Diseases (1) :OMIM:180860
 

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