Human Phenotype Ontology 
Grandparent Node:
expand
Recurrent infections (HP:0002719)help
Grandparent Node:
expand
Respiratory tract infection (HP:0011947)help
Parent Node:
expand
Recurrent respiratory infections (HP:0002205)help
..Starting node
..expand
Recurrent sinopulmonary infections (HP:0005425)help
Term ID: 5425
Name: Recurrent sinopulmonary infections
Synonym: Chronic sinopulmonary infection; Recurrent sinus and lung infections
Definition: An increased susceptibility to infections involving both the paranasal sinuses and the lungs, as manifested by a history of recurrent sinopulmonary infections.
Comments:
Reference: HP:0005425
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 streptococcus pneumoniae infections (HP:0005366) help
..expandRecurrent upper respiratory tract infections (HP:0002788) help
..expandRespiratory infections in early life (HP:0004880) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0005425HP:0005425Recurrent sinopulmonary infections0ATP6V0A2 CL E G H235452834ORPHA15630918481611716
HP:0005425HP:0005425Recurrent sinopulmonary infections0CASP8 CL E G H841607271Caspase-8 deficiency607271C1846545OMIM1121391509601763
HP:0005425HP:0005425Recurrent sinopulmonary infections0DOCK8 CL E G H81704243700Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive243700C1968689OMIM1169118119191611432
HP:0005425HP:0005425Recurrent sinopulmonary infections0NBN CL E G H4683647ORPHA114820457652602667
HP:0005425HP:0005425Recurrent sinopulmonary infections0NFKB1 CL E G H4790616576Immunodeficiency, common variable, 12616576C4225277OMIM136977794164011
HP:0005425HP:0005425Recurrent sinopulmonary infections0PIK3CD CL E G H5293615513Immunodeficiency 14615513C3714976OMIM1142228977602839
HP:0005425HP:0005425Recurrent sinopulmonary infections0STAT3 CL E G H6774147060Hyperimmunoglobulin E syndrome147060C3489795OMIM115529111364102582
HP:0005425HP:0005425Recurrent sinopulmonary infections0TNFRSF13B CL E G H23495609529Immunoglobulin A deficiency 2609529C1836032OMIM15022818153604907
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005425HP:0005425Recurrent sinopulmonary infections0TFRC CL E G H7037616740Immunodeficiency 46616740C4225219OMIM0311511763190010


Genes (9) :ATP6V0A2 CASP8 DOCK8 NBN NFKB1 PIK3CD STAT3 TFRC TNFRSF13B

Diseases (9) :2834 607271 243700 647 616576 615513 147060 616740 609529
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.