Human Phenotype Ontology 
Grandparent Node:
expand
Recurrent bacterial infections (HP:0002718)help
Parent Node:
expand
Recurrent staphylococcal infections (HP:0007499)help
..Starting node
..expand
Recurrent Staphylococcus aureus infections (HP:0002726)help
Term ID: 2726
Name: Recurrent Staphylococcus aureus infections
Synonym: Staphylococcus aureus infections, recurrent
Definition: Increased susceptibility to Staphylococcus aureus infections, as manifested by recurrent episodes of Staphylococcus aureus infection.
Comments:
Reference: HP:0002726
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:0002726HP:0002726Recurrent Staphylococcus aureus infections0CEACAM3 CL E G H10841815ORPHA:586Cystic fibrosis
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0CEACAM6 CL E G H46801818ORPHA:586Cystic fibrosis1
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0CFTR CL E G H10801884ORPHA:586Cystic fibrosis1371
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0CIITA CL E G H42617067ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent118
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0CLCA4 CL E G H228022018ORPHA:586Cystic fibrosis
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0CYBA CL E G H15352577OMIM:233690GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE.27
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0CYBB CL E G H15362578OMIM:306400Chronic granulomatous disease, X-linked.111
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0DCTN4 CL E G H5116415518ORPHA:586Cystic fibrosis
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0EDNRA CL E G H19093179ORPHA:586Cystic fibrosis3
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0FCN3 CL E G H85473625OMIM:613860FICOLIN 3 DEFICIENCY1
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0GCLC CL E G H27294311ORPHA:586Cystic fibrosis2
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0GSTM3 CL E G H29474635ORPHA:586Cystic fibrosis1
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0HFE CL E G H30774886ORPHA:586Cystic fibrosis38
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0HMOX1 CL E G H31625013ORPHA:586Cystic fibrosis3
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0IL17RA CL E G H237655985OMIM:613953Immunodeficiency 51196
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0KCNN4 CL E G H37836293ORPHA:586Cystic fibrosis3
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0MIF CL E G H42827097ORPHA:586Cystic fibrosis1
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0NCF1 CL E G H6533617660OMIM:233700Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I.13
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0NCF2 CL E G H46887661OMIM:233710Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II.67
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0NTRK1 CL E G H49148031ORPHA:642Hereditary sensory and autonomic neuropathy type 4HP:0040281 - Very frequent97
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0PGM3 CL E G H52388907OMIM:615816Immunodeficiency 2315
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0RFX5 CL E G H59939986ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent38
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0RFXANK CL E G H86259987ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent26
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0RFXAP CL E G H59949988ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent34
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0SERPINA1 CL E G H52658941ORPHA:586Cystic fibrosis131
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0SLC11A1 CL E G H655610907ORPHA:586Cystic fibrosis2
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0SLC26A9 CL E G H11501914469ORPHA:586Cystic fibrosis5
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0SLC6A14 CL E G H1125411047ORPHA:586Cystic fibrosis
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0SLC9A3 CL E G H655011073ORPHA:586Cystic fibrosis7
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0STAT3 CL E G H677411364OMIM:147060Hyper-IgE recurrent infection syndrome110
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0STX1A CL E G H680411433ORPHA:586Cystic fibrosis
HP:0002726HP:0002726Recurrent Staphylococcus aureus infections0TGFB1 CL E G H704011766ORPHA:586Cystic fibrosis13


Genes (32) :CEACAM3 CEACAM6 CFTR CIITA CLCA4 CYBA CYBB DCTN4 EDNRA FCN3 GCLC GSTM3 HFE HMOX1 IL17RA KCNN4 MIF NCF1 NCF2 NTRK1 PGM3 RFX5 RFXANK RFXAP SERPINA1 SLC11A1 SLC26A9 SLC6A14 SLC9A3 STAT3 STX1A TGFB1

Diseases (11) :ORPHA:586 ORPHA:572 OMIM:233690 OMIM:306400 OMIM:613860 OMIM:613953 OMIM:233700 OMIM:233710 ORPHA:642 OMIM:615816 OMIM:147060
 

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