Human Phenotype Ontology 
..Starting node
..expandRecurrent viral upper respiratory tract infections (HP:0033166)help
Term ID: 33166
Name: Recurrent viral upper respiratory tract infections
Synonym:
Definition: An increased susceptibility to viral upper respiratory tract infections as manifested by a history of recurrent viral upper respiratory tract infections (otitis, sinusitis, pharyngitis, tonsillitis).
Comments:
Reference: HP:0033166
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0033166HP:0033166Recurrent viral upper respiratory tract infections0FCGR3A CL E G H22143619OMIM:615707Immunodeficiency 204
HP:0033166HP:0033166Recurrent viral upper respiratory tract infections0IFIH1 CL E G H6413518873OMIM:619773IMMUNODEFICIENCY 95; IMD9528
HP:0033166HP:0033166Recurrent viral upper respiratory tract infections0NFKB2 CL E G H47917795OMIM:615577Immunodeficiency, common variable, 1011


Genes (3) :FCGR3A IFIH1 NFKB2

Diseases (3) :OMIM:615707 OMIM:619773 OMIM:615577
 

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