Tunnus
Ringing in ears
Kliiniline nimetus: Tinnitus
Tinnitus is an auditory perception that can be described as the experience of sound, in the ear or in the head, in the absence of external acoustic stimulation.
Kokkuvõte
- Teised nimetused
- Ringing in the ears
- Kehasüsteem
- Abnormality of the ear
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Ringing in ears, and the rest of your genome, with one test.
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Telli oma Genome Test59 geeni on seotud tunnusega Ringing in ears
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Ringing in ears. 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 |
|---|---|---|
| ANKHANKH inorganic pyrophosphate transport regulator | Alati | Esineb 1 haiguses |
| CTSAcathepsin A | Alati | Esineb 1 haiguses |
| THOC1THO complex subunit 1 | Alati | Esineb 1 haiguses |
| JAK2Janus kinase 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Sageli (30–79%) | Esineb 3 haiguses |
| CAV1caveolin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CCND1cyclin D1 | Sageli (30–79%) | Esineb 1 haiguses |
| DIABLOdiablo IAP-binding mitochondrial protein | Sageli (30–79%) | Esineb 1 haiguses |
| DKK1dickkopf Wnt signaling pathway inhibitor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| FASFas cell surface death receptor | Sageli (30–79%) | Esineb 1 haiguses |
| GLAgalactosidase alpha | Sageli (30–79%) | Esineb 1 haiguses |
| GRM1glutamate metabotropic receptor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MYO3Amyosin IIIA | Sageli (30–79%) | Esineb 1 haiguses |
| NAGAalpha-N-acetylgalactosaminidase | Sageli (30–79%) | Esineb 1 haiguses |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Sageli (30–79%) | Esineb 1 haiguses |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Sageli (30–79%) | Esineb 1 haiguses |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Sageli (30–79%) | Esineb 1 haiguses |
| SDHCsuccinate dehydrogenase complex subunit C | Sageli (30–79%) | Esineb 1 haiguses |
| SDHDsuccinate dehydrogenase complex subunit D | Sageli (30–79%) | Esineb 1 haiguses |
| VHLvon Hippel-Lindau tumor suppressor | Sageli (30–79%) | Esineb 1 haiguses |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP2B2ATPase plasma membrane Ca2+ transporting 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CACNA1Dcalcium voltage-gated channel subunit alpha1 D | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLCN2chloride voltage-gated channel 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COQ6coenzyme Q6, monooxygenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LZTR1leucine zipper like post translational regulator 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MIR96microRNA 96 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Mõnikord (5–29%) | Esineb 4 haiguses |
| PHEXphosphate regulating endopeptidase X-linked | Mõnikord (5–29%) | Esineb 1 haiguses |
| PMP22peripheral myelin protein 22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRRT2proline rich transmembrane protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RRP12ribosomal RNA processing 12 homolog | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| AKT1AKT serine/threonine kinase 1 | Harva (1–4%) | Esineb 1 haiguses |
Näita veel 19 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| BAP1BRCA1 associated deubiquitinase 1 | Harva (1–4%) | Esineb 1 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Harva (1–4%) | Esineb 1 haiguses |
| PDGFBplatelet derived growth factor subunit B | Harva (1–4%) | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Harva (1–4%) | Esineb 1 haiguses |
| SLC12A3solute carrier family 12 member 3 | Harva (1–4%) | Esineb 1 haiguses |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Harva (1–4%) | Esineb 1 haiguses |
| SMOsmoothened, frizzled class receptor | Harva (1–4%) | Esineb 1 haiguses |
| SUFUSUFU negative regulator of hedgehog signaling | Harva (1–4%) | Esineb 1 haiguses |
| TERTtelomerase reverse transcriptase | Harva (1–4%) | Esineb 1 haiguses |
| TRAF7TNF receptor associated factor 7 | Harva (1–4%) | Esineb 1 haiguses |
| COCHcochlin | Pole registreeritud | Esineb 1 haiguses |
| DSPPdentin sialophosphoprotein | Pole registreeritud | Esineb 1 haiguses |
| KCNQ4potassium voltage-gated channel subfamily Q member 4 | Pole registreeritud | Esineb 1 haiguses |
| MFN2mitofusin 2 | Pole registreeritud | Esineb 1 haiguses |
| OSBPL2oxysterol binding protein like 2 | Pole registreeritud | Esineb 1 haiguses |
| P2RX2purinergic receptor P2X 2 | Pole registreeritud | Esineb 1 haiguses |
| SLC39A14solute carrier family 39 member 14 | Pole registreeritud | Esineb 1 haiguses |
| SLC44A4solute carrier family 44 member 4 | Pole registreeritud | Esineb 1 haiguses |
| TMC1transmembrane channel like 1 | Pole registreeritud | 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.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast