Tunnus
Chronic rhinitis
Chronic inflammation of the nasal mucosa.
Kokkuvõte
- Kehasüsteem
- Abnormality of head or neck
Read the genes linked to Chronic rhinitis, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test66 geeni on seotud tunnusega Chronic rhinitis
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Chronic rhinitis. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| BRWD1bromodomain and WD repeat domain containing 1 | Alati | Esineb 2 haiguses |
| DNAH1dynein axonemal heavy chain 1 | Alati | Esineb 2 haiguses |
| DNAH11dynein axonemal heavy chain 11 | Alati | Esineb 2 haiguses |
| DNAH9dynein axonemal heavy chain 9 | Alati | Esineb 2 haiguses |
| DNAJB13DnaJ heat shock protein family (Hsp40) member B13 | Alati | Esineb 2 haiguses |
| DNAL1dynein axonemal light chain 1 | Alati | Esineb 2 haiguses |
| FOXJ1forkhead box J1 | Alati | Esineb 2 haiguses |
| HYDINHYDIN axonemal central pair apparatus protein | Alati | Esineb 2 haiguses |
| NLRP1NLR family pyrin domain containing 1 | Alati | Esineb 1 haiguses |
| ODAD4outer dynein arm docking complex subunit 4 | Alati | Esineb 2 haiguses |
| OSBPL2oxysterol binding protein like 2 | Alati | Esineb 1 haiguses |
| RSPH3radial spoke head 3 | Alati | Esineb 2 haiguses |
| SASH3SAM and SH3 domain containing 3 | Alati | Esineb 1 haiguses |
| TM2D3TM2 domain containing 3 | Alati | Esineb 1 haiguses |
| CLCN7Cl-/H+ antiporter 7 | Väga sageli (80–99%) | Esineb 1 haiguses |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RSPH1radial spoke head component 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| RSPH4Aradial spoke head component 4A | Väga sageli (80–99%) | Esineb 2 haiguses |
| RSPH9radial spoke head component 9 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SNX10sorting nexin 10 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TNFSF11TNF superfamily member 11 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| CCDC39coiled-coil domain 39 molecular ruler complex subunit | Sageli (30–79%) | Esineb 1 haiguses |
| CCDC40coiled-coil domain 40 molecular ruler complex subunit | Sageli (30–79%) | Esineb 1 haiguses |
| CCNOcyclin O | Sageli (30–79%) | Esineb 1 haiguses |
| CFAP221cilia and flagella associated protein 221 | Sageli (30–79%) | Esineb 1 haiguses |
| CFAP298cilia and flagella associated protein 298 | Sageli (30–79%) | Esineb 1 haiguses |
| CFAP300cilia and flagella associated protein 300 | Sageli (30–79%) | Esineb 1 haiguses |
| CFAP74cilia and flagella associated protein 74 | Sageli (30–79%) | Esineb 1 haiguses |
| CLXNcalaxin | Sageli (30–79%) | Esineb 1 haiguses |
| DAW1dynein assembly factor with WD repeats 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF1dynein axonemal assembly factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF11dynein axonemal assembly factor 11 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF19dynein axonemal assembly factor 19 | Sageli (30–79%) | Esineb 2 haiguses |
| DNAAF2dynein axonemal assembly factor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF3dynein axonemal assembly factor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF4dynein axonemal assembly factor 4 | Sageli (30–79%) | Esineb 2 haiguses |
| DNAAF5dynein axonemal assembly factor 5 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF6dynein axonemal assembly factor 6 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 26 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| DNAH5dynein axonemal heavy chain 5 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAH7dynein axonemal heavy chain 7 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAI1dynein axonemal intermediate chain 1 | Sageli (30–79%) | Esineb 2 haiguses |
| DNAI2dynein axonemal intermediate chain 2 | Sageli (30–79%) | Esineb 2 haiguses |
| DRC1dynein regulatory complex subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DRC2dynein regulatory complex subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| DRC4dynein regulatory complex subunit 4 | Sageli (30–79%) | Esineb 2 haiguses |
| GAS2L2growth arrest specific 2 like 2 | Sageli (30–79%) | Esineb 1 haiguses |
| LRRC56leucine rich repeat containing 56 | Sageli (30–79%) | Esineb 1 haiguses |
| MCIDASmulticiliate differentiation and DNA synthesis associated cell cycle protein | Sageli (30–79%) | Esineb 2 haiguses |
| NEK10NIMA related kinase 10 | Sageli (30–79%) | Esineb 1 haiguses |
| NME5NME/NM23 family member 5 | Sageli (30–79%) | Esineb 1 haiguses |
| NME8NME/NM23 family member 8 | Sageli (30–79%) | Esineb 1 haiguses |
| ODAD1outer dynein arm docking complex subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ODAD2outer dynein arm docking complex subunit 2 | Sageli (30–79%) | Esineb 2 haiguses |
| ODAD3outer dynein arm docking complex subunit 3 | Sageli (30–79%) | Esineb 1 haiguses |
| OFD1OFD1 centriole and centriolar satellite protein | Sageli (30–79%) | Esineb 1 haiguses |
| RPGRretinitis pigmentosa GTPase regulator | Sageli (30–79%) | Esineb 1 haiguses |
| SPAG1sperm associated antigen 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SPEF2sperm flagellar and cilia associated 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SPINK5serine peptidase inhibitor Kazal type 5 | Sageli (30–79%) | Esineb 1 haiguses |
| STK36serine/threonine kinase 36 | Sageli (30–79%) | Esineb 1 haiguses |
| TAP2transporter 2, ATP binding cassette subfamily B member | Sageli (30–79%) | Esineb 1 haiguses |
| TTC12tetratricopeptide repeat domain 12 | Sageli (30–79%) | Esineb 2 haiguses |
| ZMYND10zinc finger MYND-type containing 10 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC29A3solute carrier family 29 member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Kitsamad tunnused
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.16-c6eea6bf.
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Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast