Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the gastrointestinal tract (HP:0011024)help
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Neoplasm of the gastrointestinal tract (HP:0007378)help
..Starting node
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Benign gastrointestinal tract tumors (HP:0006719)help
Term ID: 6719
Name: Benign gastrointestinal tract tumors
Synonym: Benign gastrointestinal tract tumours; Benign GI tract tumors; Benign GI tract tumours; Non-cancerous GI tumors; Non-cancerous GI tumours
Definition:
Comments:
Reference: HP:0006719
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAmpulla of Vater carcinoma (HP:0031524) help
..expandBiliary tract neoplasm (HP:0100574) help
..expandDesmoid tumors (HP:0100245) help
..expandEsophageal neoplasm (HP:0100751) help
..expandGastrointestinal stroma tumor (HP:0100723) help
..expandIntestinal carcinoid (HP:0006723) help
..expandIntestinal polyp (HP:0005266) help
..expandMalignant gastrointestinal tract tumors (HP:0006749) help
..expandMultiple intestinal neurofibromatosis (HP:0005220) help
..expandNeoplasm of the large intestine (HP:0100834) help
..expandNeoplasm of the liver (HP:0002896) help
..expandNeoplasm of the small intestine (HP:0100833) help
..expandNeoplasm of the stomach (HP:0006753) help
..expandPrimary peritoneal carcinoma (HP:0030406) help
..expandZollinger-Ellison syndrome (HP:0002044) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0006719HP:0006719Benign gastrointestinal tract tumors0MLH1 CL E G H4292158320Muir-Torré syndrome158320C1321489OMIM137637127120436
HP:0006719HP:0006719Benign gastrointestinal tract tumors0MLH1 CL E G H4292158320Muir-Torré syndrome158320C1321489OMIM135407127120436
HP:0006719HP:0006719Benign gastrointestinal tract tumors0MSH2 CL E G H4436158320Muir-Torré syndrome158320C1321489OMIM149647325609309
HP:0006719HP:0006719Benign gastrointestinal tract tumors0MSH2 CL E G H4436158320Muir-Torré syndrome158320C1321489OMIM146077325609309
 
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 August 2021 release.