Human Phenotype Ontology 
Grandparent Node:
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Recurrent infections (HP:0002719)help
Grandparent Node:
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Respiratory tract infection (HP:0011947)help
Parent Node:
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Recurrent respiratory infections (HP:0002205)help
..Starting node
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Recurrent streptococcus pneumoniae infections (HP:0005366)help
Term ID: 5366
Name: Recurrent streptococcus pneumoniae infections
Synonym:
Definition: Increased susceptibility to streptococcus pneumoniae infections as manifested by a history of recurrent infections by streptococcus pneumoniae.
Comments:
Reference: HP:0005366
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandRecurrent bronchopulmonary infections (HP:0006538) help
..expandRecurrent infections due to aspiration (HP:0004891) help
..expandRecurrent lower respiratory tract infections (HP:0002783) help
..expandRecurrent sinopulmonary infections (HP:0005425) help
..expandRecurrent upper respiratory tract infections (HP:0002788) help
..expandRespiratory infections in early life (HP:0004880) 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:0005366HP:0005366Recurrent streptococcus pneumoniae infections0CFI CL E G H34265394OMIM:610984Complement factor I deficiency.57
HP:0005366HP:0005366Recurrent streptococcus pneumoniae infections0IRAK4 CL E G H5113517967ORPHA:70592Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiencyHP:0040281 - Very frequent58


Genes (2) :CFI IRAK4

Diseases (2) :OMIM:610984 ORPHA:70592
 

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