Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of immune system physiology (HP:0010978)help
Parent Node:
expandAbnormality of the middle ear (HP:0000370)help
Parent Node:
expandRecurrent infections (HP:0002719)help
..Starting node
..expandRecurrent infections of the middle ear (HP:0040268)help
Term ID: 40268
Name: Recurrent infections of the middle ear
Synonym:
Definition: Increased susceptibility to middle ear infections, as manifested by recurrent episodes of middle ear infections
Comments:
Reference: HP:0040268
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFailure to thrive secondary to recurrent infections (HP:0008866) help
..expandRecurrent abscess formation (HP:0002722) help
..expandRecurrent bacterial infections (HP:0002718) help
..expandRecurrent ear infections (HP:0410018) help
..expandRecurrent fungal infections (HP:0002841) help
..expandRecurrent infection of the gastrointestinal tract (HP:0004798) help
..expandRecurrent infections in infancy and early childhood (HP:0005437) help
..expandRecurrent opportunistic infections (HP:0005390) help
..expandRecurrent otitis media (HP:0000403) help
..expandRecurrent parasitic infections (HP:0030885) help
..expandRecurrent protozoan infections (HP:0005386) help
..expandRecurrent respiratory infections (HP:0002205) help
..expandRecurrent urinary tract infections (HP:0000010) help
..expandRecurrent viral infections (HP:0004429) 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:0040268HP:0040268Recurrent infections of the middle ear0EYA4 CL E G H20703522ORPHA:217622Sensorineural deafness with dilated cardiomyopathyHP:0040281 - Very frequent111


Genes (1) :EYA4

Diseases (1) :ORPHA:217622
 

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