Human Phenotype Ontology 
Grandparent Node:
expand
Recurrent bacterial infections (HP:0002718)help
Parent Node:
expand
Recurrent gram-negative bacterial infections (HP:0005420)help
..Starting node
..expand
Recurrent Burkholderia cepacia infections (HP:0002842)help
Term ID: 2842
Name: Recurrent Burkholderia cepacia infections
Synonym:
Definition: Increased susceptibility to infections with Burkholderia cepacia, as manifested by recurrent episodes of infection with this agent.
Comments:
Reference: HP:0002842
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandRecurrent E. coli infections (HP:0002740) help
..expandRecurrent Haemophilus influenzae infections (HP:0005376) help
..expandRecurrent Klebsiella infections (HP:0002742) help
..expandRecurrent Neisserial infections (HP:0005430) help
..expandRecurrent Serratia marcescens infections (HP:0002741) 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:0002842HP:0002842Recurrent Burkholderia cepacia infections0CEACAM3 CL E G H10841815ORPHA:586Cystic fibrosis
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0CEACAM6 CL E G H46801818ORPHA:586Cystic fibrosis1
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0CFTR CL E G H10801884ORPHA:586Cystic fibrosis1371
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0CLCA4 CL E G H228022018ORPHA:586Cystic fibrosis
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0CYBA CL E G H15352577OMIM:233690GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE.27
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0CYBB CL E G H15362578OMIM:306400Chronic granulomatous disease, X-linked.111
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0DCTN4 CL E G H5116415518ORPHA:586Cystic fibrosis
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0EDNRA CL E G H19093179ORPHA:586Cystic fibrosis3
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0GCLC CL E G H27294311ORPHA:586Cystic fibrosis2
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0GSTM3 CL E G H29474635ORPHA:586Cystic fibrosis1
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0HFE CL E G H30774886ORPHA:586Cystic fibrosis38
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0HMOX1 CL E G H31625013ORPHA:586Cystic fibrosis3
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0KCNN4 CL E G H37836293ORPHA:586Cystic fibrosis3
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0MIF CL E G H42827097ORPHA:586Cystic fibrosis1
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0NCF1 CL E G H6533617660OMIM:233700Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I.13
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0NCF2 CL E G H46887661OMIM:233710Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II.67
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0SERPINA1 CL E G H52658941ORPHA:586Cystic fibrosis131
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0SLC11A1 CL E G H655610907ORPHA:586Cystic fibrosis2
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0SLC26A9 CL E G H11501914469ORPHA:586Cystic fibrosis5
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0SLC6A14 CL E G H1125411047ORPHA:586Cystic fibrosis
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0SLC9A3 CL E G H655011073ORPHA:586Cystic fibrosis7
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0STX1A CL E G H680411433ORPHA:586Cystic fibrosis
HP:0002842HP:0002842Recurrent Burkholderia cepacia infections0TGFB1 CL E G H704011766ORPHA:586Cystic fibrosis13


Genes (23) :CEACAM3 CEACAM6 CFTR CLCA4 CYBA CYBB DCTN4 EDNRA GCLC GSTM3 HFE HMOX1 KCNN4 MIF NCF1 NCF2 SERPINA1 SLC11A1 SLC26A9 SLC6A14 SLC9A3 STX1A TGFB1

Diseases (5) :ORPHA:586 OMIM:233690 OMIM:306400 OMIM:233700 OMIM:233710
 

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