Human Phenotype Ontology 
Grandparent Node:
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Recurrent infections (HP:0002719)help
Parent Node:
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Recurrent bacterial infections (HP:0002718)help
..Starting node
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Recurrent staphylococcal infections (HP:0007499)help
Term ID: 7499
Name: Recurrent staphylococcal infections
Synonym: Recurrent staphylococcal infections
Definition: Increased susceptibility to staphylococcal infections, as manifested by recurrent episodes of staphylococcal infections.
Comments:
Reference: HP:0007499
Genes and Diseases:
 
       Child Nodes:
........expandRecurrent Staphylococcus aureus infections (HP:0002726) help

 Sister Nodes: 
..expandRecurrent bacterial skin infections (HP:0005406) help
..expandRecurrent gram-negative bacterial infections (HP:0005420) help
..expandRecurrent mycobacterial infections (HP:0011274) help
..expandRecurrent systemic pyogenic infections (HP:0005429) 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:0007499HP:0007499Recurrent staphylococcal infections0CEACAM3 CL E G H10841815ORPHA:586Cystic fibrosis
HP:0007499HP:0007499Recurrent staphylococcal infections0CEACAM6 CL E G H46801818ORPHA:586Cystic fibrosis1
HP:0007499HP:0007499Recurrent staphylococcal infections0CFTR CL E G H10801884ORPHA:586Cystic fibrosis1371
HP:0007499HP:0007499Recurrent staphylococcal infections0CIITA CL E G H42617067ORPHA:572Immunodeficiency by defective expression of MHC class II118
HP:0007499HP:0007499Recurrent staphylococcal infections0CLCA4 CL E G H228022018ORPHA:586Cystic fibrosis
HP:0007499HP:0007499Recurrent staphylococcal infections0CYBA CL E G H15352577OMIM:233690GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE27
HP:0007499HP:0007499Recurrent staphylococcal infections0CYBB CL E G H15362578OMIM:306400Chronic granulomatous disease, X-linked111
HP:0007499HP:0007499Recurrent staphylococcal infections0DCTN4 CL E G H5116415518ORPHA:586Cystic fibrosis
HP:0007499HP:0007499Recurrent staphylococcal infections0EDNRA CL E G H19093179ORPHA:586Cystic fibrosis3
HP:0007499HP:0007499Recurrent staphylococcal infections0FCN3 CL E G H85473625OMIM:613860FICOLIN 3 DEFICIENCY1
HP:0007499HP:0007499Recurrent staphylococcal infections0GCLC CL E G H27294311ORPHA:586Cystic fibrosis2
HP:0007499HP:0007499Recurrent staphylococcal infections0GSTM3 CL E G H29474635ORPHA:586Cystic fibrosis1
HP:0007499HP:0007499Recurrent staphylococcal infections0HFE CL E G H30774886ORPHA:586Cystic fibrosis38
HP:0007499HP:0007499Recurrent staphylococcal infections0HMOX1 CL E G H31625013ORPHA:586Cystic fibrosis3
HP:0007499HP:0007499Recurrent staphylococcal infections0IL17RA CL E G H237655985OMIM:613953Immunodeficiency 51196
HP:0007499HP:0007499Recurrent staphylococcal infections0IRAK4 CL E G H5113517967OMIM:607676Immunodeficiency 6758
HP:0007499HP:0007499Recurrent staphylococcal infections0IRAK4 CL E G H5113517967ORPHA:70592Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiencyHP:0040281 - Very frequent58
HP:0007499HP:0007499Recurrent staphylococcal infections0ITGB2 CL E G H36896155OMIM:116920Leukocyte adhesion deficiency, type I.114
HP:0007499HP:0007499Recurrent staphylococcal infections0KCNN4 CL E G H37836293ORPHA:586Cystic fibrosis3
HP:0007499HP:0007499Recurrent staphylococcal infections0LYST CL E G H11301968ORPHA:167Chédiak-Higashi syndromeHP:0040282 - Frequent239
HP:0007499HP:0007499Recurrent staphylococcal infections0MIF CL E G H42827097ORPHA:586Cystic fibrosis1
HP:0007499HP:0007499Recurrent staphylococcal infections0NCF1 CL E G H6533617660OMIM:233700Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I13
HP:0007499HP:0007499Recurrent staphylococcal infections0NCF2 CL E G H46887661OMIM:233710Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II67
HP:0007499HP:0007499Recurrent staphylococcal infections0NTRK1 CL E G H49148031ORPHA:642Hereditary sensory and autonomic neuropathy type 497
HP:0007499HP:0007499Recurrent staphylococcal infections0PGM3 CL E G H52388907OMIM:615816Immunodeficiency 2315
HP:0007499HP:0007499Recurrent staphylococcal infections0RFX5 CL E G H59939986ORPHA:572Immunodeficiency by defective expression of MHC class II38
HP:0007499HP:0007499Recurrent staphylococcal infections0RFXANK CL E G H86259987ORPHA:572Immunodeficiency by defective expression of MHC class II26
HP:0007499HP:0007499Recurrent staphylococcal infections0RFXAP CL E G H59949988ORPHA:572Immunodeficiency by defective expression of MHC class II34
HP:0007499HP:0007499Recurrent staphylococcal infections0SERPINA1 CL E G H52658941ORPHA:586Cystic fibrosis131
HP:0007499HP:0007499Recurrent staphylococcal infections0SLC11A1 CL E G H655610907ORPHA:586Cystic fibrosis2
HP:0007499HP:0007499Recurrent staphylococcal infections0SLC26A9 CL E G H11501914469ORPHA:586Cystic fibrosis5
HP:0007499HP:0007499Recurrent staphylococcal infections0SLC6A14 CL E G H1125411047ORPHA:586Cystic fibrosis
HP:0007499HP:0007499Recurrent staphylococcal infections0SLC9A3 CL E G H655011073ORPHA:586Cystic fibrosis7
HP:0007499HP:0007499Recurrent staphylococcal infections0STAT3 CL E G H677411364OMIM:147060Hyper-IgE recurrent infection syndrome110
HP:0007499HP:0007499Recurrent staphylococcal infections0STX1A CL E G H680411433ORPHA:586Cystic fibrosis
HP:0007499HP:0007499Recurrent staphylococcal infections0TGFB1 CL E G H704011766ORPHA:586Cystic fibrosis13
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1CEACAM3 CL E G H10841815ORPHA:586Cystic fibrosis
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1CEACAM6 CL E G H46801818ORPHA:586Cystic fibrosis1
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1CFTR CL E G H10801884ORPHA:586Cystic fibrosis1371
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1CIITA CL E G H42617067ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent118
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1CLCA4 CL E G H228022018ORPHA:586Cystic fibrosis
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1CYBA CL E G H15352577OMIM:233690GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE.27
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1CYBB CL E G H15362578OMIM:306400Chronic granulomatous disease, X-linked.111
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1DCTN4 CL E G H5116415518ORPHA:586Cystic fibrosis
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1EDNRA CL E G H19093179ORPHA:586Cystic fibrosis3
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1FCN3 CL E G H85473625OMIM:613860FICOLIN 3 DEFICIENCY1
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1GCLC CL E G H27294311ORPHA:586Cystic fibrosis2
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1GSTM3 CL E G H29474635ORPHA:586Cystic fibrosis1
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1HFE CL E G H30774886ORPHA:586Cystic fibrosis38
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1HMOX1 CL E G H31625013ORPHA:586Cystic fibrosis3
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1IL17RA CL E G H237655985OMIM:613953Immunodeficiency 51196
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1KCNN4 CL E G H37836293ORPHA:586Cystic fibrosis3
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1MIF CL E G H42827097ORPHA:586Cystic fibrosis1
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1NCF1 CL E G H6533617660OMIM:233700Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I.13
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1NCF2 CL E G H46887661OMIM:233710Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II.67
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1NTRK1 CL E G H49148031ORPHA:642Hereditary sensory and autonomic neuropathy type 4HP:0040281 - Very frequent97
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1PGM3 CL E G H52388907OMIM:615816Immunodeficiency 2315
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1RFX5 CL E G H59939986ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent38
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1RFXANK CL E G H86259987ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent26
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1RFXAP CL E G H59949988ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent34
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1SERPINA1 CL E G H52658941ORPHA:586Cystic fibrosis131
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1SLC11A1 CL E G H655610907ORPHA:586Cystic fibrosis2
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1SLC26A9 CL E G H11501914469ORPHA:586Cystic fibrosis5
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1SLC6A14 CL E G H1125411047ORPHA:586Cystic fibrosis
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1SLC9A3 CL E G H655011073ORPHA:586Cystic fibrosis7
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1STAT3 CL E G H677411364OMIM:147060Hyper-IgE recurrent infection syndrome110
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1STX1A CL E G H680411433ORPHA:586Cystic fibrosis
HP:0007499HP:0002726Recurrent Staphylococcus aureus infections1TGFB1 CL E G H704011766ORPHA:586Cystic fibrosis13


Genes (35) :CEACAM3 CEACAM6 CFTR CIITA CLCA4 CYBA CYBB DCTN4 EDNRA FCN3 GCLC GSTM3 HFE HMOX1 IL17RA IRAK4 ITGB2 KCNN4 LYST MIF NCF1 NCF2 NTRK1 PGM3 RFX5 RFXANK RFXAP SERPINA1 SLC11A1 SLC26A9 SLC6A14 SLC9A3 STAT3 STX1A TGFB1

Diseases (15) :ORPHA:586 ORPHA:572 OMIM:233690 OMIM:306400 OMIM:613860 OMIM:613953 OMIM:607676 ORPHA:70592 OMIM:116920 ORPHA:167 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.