Human Phenotype Ontology 
Grandparent Node:
expand
Neoplasm of the skin (HP:0008069)help
Parent Node:
expand
Abnormal choroid plexus morphology (HP:0007376)help
Parent Node:
expand
Benign neoplasm of the central nervous system (HP:0100835)help
Parent Node:
expand
Papilloma (HP:0012740)help
..Starting node
..expand
Choroid plexus papilloma (HP:0200022)help
Term ID: 200022
Name: Choroid plexus papilloma
Synonym:
Definition: Choroid plexus papilloma is a histologically benign neoplasm located in the ventricular system of the choroid plexus.
Comments:
Reference: HP:0200022
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFacial papilloma (HP:0040167) help
..expandSquamous Papilloma (HP:0031021) help
..expandVerrucae (HP:0200043) 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:0200022HP:0200022Choroid plexus papilloma0NRAS CL E G H48937989OMIM:249400Neurocutaneous melanosis, somaticHP:0040283 - Occasional102
HP:0200022HP:0200022Choroid plexus papilloma0TP53 CL E G H715711998OMIM:260500Papilloma of choroid plexus.911
HP:0200022HP:0200022Choroid plexus papilloma0TP53 CL E G H715711998ORPHA:2807Papilloma of choroid plexusHP:0040281 - Very frequent911


Genes (2) :NRAS TP53

Diseases (3) :OMIM:249400 OMIM:260500 ORPHA:2807
 

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