Human Phenotype Ontology 
Grandparent Node:
expandRenal cell carcinoma (HP:0005584)help
Parent Node:
expandPapillary renal cell carcinoma (HP:0006766)help
..Starting node
..expandPapillary renal cell carcinoma type 2 (HP:0006732)help
Term ID: 6732
Name: Papillary renal cell carcinoma type 2
Synonym:
Definition: A type of papillary renal cell carcinoma in which the papillae are covered by large eosinophilic cells with pleomorphic nuclei, prominent nucleoli, and nuclear pseudostratification.
Comments:
Reference: HP:0006732
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPapillary renal cell carcinoma type 1 (HP:0011797) 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:0006732HP:0006732Papillary renal cell carcinoma type 20FH CL E G H22713700ORPHA:523Hereditary leiomyomatosis and renal cell cancerHP:0040283 - Occasional301


Genes (1) :FH

Diseases (1) :ORPHA:523
 

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