Human Phenotype Ontology 
Grandparent Node:
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Functional abnormality of the gastrointestinal tract (HP:0012719)help
Grandparent Node:
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Recurrent infections (HP:0002719)help
Parent Node:
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Recurrent infection of the gastrointestinal tract (HP:0004798)help
..Starting node
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Helicobacter pylori infection (HP:0005202)help
Term ID: 5202
Name: Helicobacter pylori infection
Synonym:
Definition: A recurrent infection of the GI tract with helicobacter pylori, a gram-negative, microaerophilic bacterium usually found in the stomach.
Comments:
Reference: HP:0005202
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFrequent Giardia lamblia infestation (HP:0005215) help
..expandRecurrent gastroenteritis (HP:0031123) 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:0005202HP:0005202Helicobacter pylori infection0CARMIL2 CL E G H14620627089OMIM:618131IMMUNODEFICIENCY 58; IMD583
HP:0005202HP:0005202Helicobacter pylori infection0CORIN CL E G H1069919012ORPHA:275555PreeclampsiaHP:0040284 - Very rare5
HP:0005202HP:0005202Helicobacter pylori infection0FLT1 CL E G H23213763ORPHA:275555PreeclampsiaHP:0040284 - Very rare11
HP:0005202HP:0005202Helicobacter pylori infection0IFNGR1 CL E G H34595439OMIM:600263Helicobacter pylori infection, susceptibility to.60
HP:0005202HP:0005202Helicobacter pylori infection0STOX1 CL E G H21973623508ORPHA:275555PreeclampsiaHP:0040284 - Very rare2


Genes (5) :CARMIL2 CORIN FLT1 IFNGR1 STOX1

Diseases (3) :OMIM:618131 ORPHA:275555 OMIM:600263
 

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