Trait
Recurrent bronchitis
An increased susceptibility to bronchitis as manifested by a history of recurrent bronchitis.
Summary
- Also called
- Bronchitis, recurrent
Reference genomeGRCh38hg38
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Get my Genome Test34 genes linked to Recurrent bronchitis
Changes in these genes cause rare conditions in which Recurrent bronchitis is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| CD19CD19 molecule | Always | In 1 condition |
| CD79ACD79a molecule | Always | In 1 condition |
| CD79BCD79b molecule | Always | In 1 condition |
| CFAP54cilia and flagella associated protein 54 | Always | In 1 condition |
| CR2complement C3d receptor 2 | Always | In 1 condition |
| DNAAF1dynein axonemal assembly factor 1 | Always | In 1 condition |
| DNAI1dynein axonemal intermediate chain 1 | Always | In 1 condition |
| DPP9dipeptidyl peptidase 9 | Always | In 1 condition |
| ICOSinducible T cell costimulator | Always | In 2 conditions |
| ICOSLGinducible T cell costimulator ligand | Always | In 1 condition |
| IL10RBinterleukin 10 receptor subunit beta | Always | In 1 condition |
| MAGT1magnesium transporter 1 | Always | In 1 condition |
| NHEJ1non-homologous end joining factor 1 | Always | In 1 condition |
| SGSM3small G protein signaling modulator 3 | Always | In 1 condition |
| TAFAZZINtafazzin, phospholipid-lysophospholipid transacylase | Always | In 1 condition |
| TNFRSF13BTNF receptor superfamily member 13B | Always | In 1 condition |
| TNFRSF13CTNF receptor superfamily member 13C | Always | In 1 condition |
| NFKB2nuclear factor kappa B subunit 2 | Very often (80–99%) | In 1 condition |
| DNAJB13DnaJ heat shock protein family (Hsp40) member B13 | Often (30–79%) | In 1 condition |
| NBNnibrin | Often (30–79%) | In 1 condition |
| RNU4-2RNA, U4 small nuclear 2 | Often (30–79%) | In 1 condition |
| DOCK11dedicator of cytokinesis 11 | Sometimes (5–29%) | In 1 condition |
| IL17RAinterleukin 17 receptor A | Sometimes (5–29%) | In 1 condition |
| RFX7regulatory factor X7 | Sometimes (5–29%) | In 1 condition |
| SEC61A1SEC61 translocon subunit alpha 1 | Sometimes (5–29%) | In 1 condition |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Sometimes (5–29%) | In 1 condition |
| ATMATM serine/threonine kinase | Not recorded | In 1 condition |
| CFAP221cilia and flagella associated protein 221 | Not recorded | In 1 condition |
| DRC4dynein regulatory complex subunit 4 | Not recorded | In 1 condition |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Not recorded | In 1 condition |
| IL2RGinterleukin 2 receptor subunit gamma | Not recorded | In 1 condition |
| MGPmatrix Gla protein | Not recorded | In 1 condition |
| RPGRretinitis pigmentosa GTPase regulator | Not recorded | In 1 condition |
| TAP1transporter 1, ATP binding cassette subfamily B member | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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