Trait
Chronic sinus disease
Clinical name: Chronic sinusitis
A chronic form of sinusitis.
Reference genomeGRCh38hg38
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Get my Genome Test72 genes linked to Chronic sinus disease
Changes in these genes cause rare conditions in which Chronic sinus disease 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 |
|---|---|---|
| BLNKB cell linker | Always | In 1 condition |
| CCDC39coiled-coil domain 39 molecular ruler complex subunit | Always | In 2 conditions |
| CD79BCD79b molecule | Always | In 1 condition |
| CFAP45cilia and flagella associated protein 45 | Always | In 1 condition |
| CFAP52cilia and flagella associated protein 52 | Always | In 1 condition |
| DNAAF2dynein axonemal assembly factor 2 | Always | In 2 conditions |
| DNAH7dynein axonemal heavy chain 7 | Always | In 2 conditions |
| DNAH9dynein axonemal heavy chain 9 | Always | In 2 conditions |
| DNAI1dynein axonemal intermediate chain 1 | Always | In 2 conditions |
| DNAI2dynein axonemal intermediate chain 2 | Always | In 2 conditions |
| FOXJ1forkhead box J1 | Always | In 2 conditions |
| ODAD4outer dynein arm docking complex subunit 4 | Always | In 2 conditions |
| RSPH3radial spoke head 3 | Always | In 2 conditions |
| SASH3SAM and SH3 domain containing 3 | Always | In 1 condition |
| TAP2transporter 2, ATP binding cassette subfamily B member | Always | In 1 condition |
| WFDC2WAP four-disulfide core domain 2 | Always | In 1 condition |
| CCDC40coiled-coil domain 40 molecular ruler complex subunit | Very often (80–99%) | In 2 conditions |
| RSPH9radial spoke head component 9 | Very often (80–99%) | In 2 conditions |
| BRWD1bromodomain and WD repeat domain containing 1 | Often (30–79%) | In 1 condition |
| CCNOcyclin O | Often (30–79%) | In 1 condition |
| CFAP221cilia and flagella associated protein 221 | Often (30–79%) | In 1 condition |
| CFAP298cilia and flagella associated protein 298 | Often (30–79%) | In 1 condition |
| CFAP300cilia and flagella associated protein 300 | Often (30–79%) | In 2 conditions |
| CFAP74cilia and flagella associated protein 74 | Often (30–79%) | In 1 condition |
| CFTRCF transmembrane conductance regulator | Often (30–79%) | In 1 condition |
| CLXNcalaxin | Often (30–79%) | In 2 conditions |
| DAW1dynein assembly factor with WD repeats 1 | Often (30–79%) | In 1 condition |
| DNAAF1dynein axonemal assembly factor 1 | Often (30–79%) | In 1 condition |
| DNAAF11dynein axonemal assembly factor 11 | Often (30–79%) | In 1 condition |
| DNAAF19dynein axonemal assembly factor 19 | Often (30–79%) | In 2 conditions |
| DNAAF3dynein axonemal assembly factor 3 | Often (30–79%) | In 1 condition |
| DNAAF4dynein axonemal assembly factor 4 | Often (30–79%) | In 1 condition |
| DNAAF5dynein axonemal assembly factor 5 | Often (30–79%) | In 1 condition |
| DNAAF6dynein axonemal assembly factor 6 | Often (30–79%) | In 1 condition |
| DNAH1dynein axonemal heavy chain 1 | Often (30–79%) | In 1 condition |
| DNAH11dynein axonemal heavy chain 11 | Often (30–79%) | In 1 condition |
| DNAH5dynein axonemal heavy chain 5 | Often (30–79%) | In 1 condition |
| DNAJB13DnaJ heat shock protein family (Hsp40) member B13 | Often (30–79%) | In 1 condition |
| DNAL1dynein axonemal light chain 1 | Often (30–79%) | In 2 conditions |
| DRC1dynein regulatory complex subunit 1 | Often (30–79%) | In 2 conditions |
Show 32 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| DRC2dynein regulatory complex subunit 2 | Often (30–79%) | In 2 conditions |
| DRC4dynein regulatory complex subunit 4 | Often (30–79%) | In 1 condition |
| FCGR2AFc gamma receptor IIa | Often (30–79%) | In 1 condition |
| GAS2L2growth arrest specific 2 like 2 | Often (30–79%) | In 1 condition |
| HYDINHYDIN axonemal central pair apparatus protein | Often (30–79%) | In 1 condition |
| LRRC56leucine rich repeat containing 56 | Often (30–79%) | In 1 condition |
| MCIDASmulticiliate differentiation and DNA synthesis associated cell cycle protein | Often (30–79%) | In 1 condition |
| NEK10NIMA related kinase 10 | Often (30–79%) | In 1 condition |
| NME5NME/NM23 family member 5 | Often (30–79%) | In 1 condition |
| NME8NME/NM23 family member 8 | Often (30–79%) | In 1 condition |
| ODAD1outer dynein arm docking complex subunit 1 | Often (30–79%) | In 1 condition |
| ODAD2outer dynein arm docking complex subunit 2 | Often (30–79%) | In 1 condition |
| ODAD3outer dynein arm docking complex subunit 3 | Often (30–79%) | In 2 conditions |
| OFD1OFD1 centriole and centriolar satellite protein | Often (30–79%) | In 1 condition |
| RNF168ring finger protein 168 | Often (30–79%) | In 1 condition |
| RPGRretinitis pigmentosa GTPase regulator | Often (30–79%) | In 2 conditions |
| RSPH1radial spoke head component 1 | Often (30–79%) | In 1 condition |
| RSPH4Aradial spoke head component 4A | Often (30–79%) | In 1 condition |
| SPAG1sperm associated antigen 1 | Often (30–79%) | In 1 condition |
| SPEF2sperm flagellar and cilia associated 2 | Often (30–79%) | In 1 condition |
| STK36serine/threonine kinase 36 | Often (30–79%) | In 1 condition |
| TGFB1transforming growth factor beta 1 | Often (30–79%) | In 1 condition |
| TTC12tetratricopeptide repeat domain 12 | Often (30–79%) | In 1 condition |
| ZMYND10zinc finger MYND-type containing 10 | Often (30–79%) | In 1 condition |
| AIREautoimmune regulator | Sometimes (5–29%) | In 1 condition |
| CSPP1centrosome and spindle pole associated protein 1 | Sometimes (5–29%) | In 1 condition |
| IGHG2immunoglobulin heavy constant gamma 2 (G2m marker) | Sometimes (5–29%) | In 1 condition |
| IGKCimmunoglobulin kappa constant | Sometimes (5–29%) | In 1 condition |
| LIG4DNA ligase 4 | Sometimes (5–29%) | In 1 condition |
| PGM3phosphoglucomutase 3 | Sometimes (5–29%) | In 1 condition |
| MGPmatrix Gla protein | 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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