Human Phenotype Ontology 
Grandparent Node:
Abnormality of the genitourinary system (HP:0000119)help
Grandparent Node:
Neoplasm by anatomical site (HP:0011793)help
Parent Node:
Neoplasm of the genitourinary tract (HP:0007379)help
..Starting node
Benign genitourinary tract neoplasm (HP:0006778)help
Term ID: 6778
Name: Benign genitourinary tract neoplasm
Synonym: Benign genitourinary tract tumor; Benign GU tract neoplasm
Definition: A non-malignant neoplasm of the genitourinary system.
Reference: HP:0006778
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandGenital neoplasm (HP:0010787) help
..expandMalignant genitourinary tract tumor (HP:0006758) help
..expandUrinary tract neoplasm (HP:0010786) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HP:0006778HP:0006778Benign genitourinary tract neoplasm0MLH1 CL E G H4292158320Muir-Torré syndrome158320C1321489OMIM112037127120436
HP:0006778HP:0006778Benign genitourinary tract neoplasm0MSH2 CL E G H4436158320Muir-Torré syndrome158320C1321489OMIM112647325609309
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (2) :MLH1 MSH2

Diseases (1) :158320

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.