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Tunnus
Hoarse voice
Hoarseness refers to a change in the pitch or quality of the voice, with the voice sounding weak, very breathy, scratchy, or husky.
Kokkuvõte
- Teised nimetused
- Hoarseness, Husky voice
- Kehasüsteem
- Abnormality of the voice
Hoarse voiceHP:0001609
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Read the genes linked to Hoarse voice, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test104 geeni on seotud tunnusega Hoarse voice
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Hoarse voice. 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 |
|---|---|---|
| APOA1apolipoprotein A1 | Alati | Esineb 1 haiguses |
| ASAH1N-acylsphingosine amidohydrolase 1 | Alati | Esineb 3 haiguses |
| CD40LGCD40 ligand | Alati | Esineb 1 haiguses |
| ECM1extracellular matrix protein 1 | Alati | Esineb 2 haiguses |
| KRT14keratin 14 | Alati | Esineb 2 haiguses |
| KRT5keratin 5 | Alati | Esineb 2 haiguses |
| LTBP3latent transforming growth factor beta binding protein 3 | Alati | Esineb 2 haiguses |
| NLRP1NLR family pyrin domain containing 1 | Alati | Esineb 1 haiguses |
| POU1F1POU class 1 homeobox 1 | Alati | Esineb 1 haiguses |
| SMSspermine synthase | Alati | Esineb 1 haiguses |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Väga sageli (80–99%) | Esineb 1 haiguses |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| CLIP2CAP-Gly domain containing linker protein 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Väga sageli (80–99%) | Esineb 1 haiguses |
| EIF4Heukaryotic translation initiation factor 4H | Väga sageli (80–99%) | Esineb 1 haiguses |
| ELNelastin | Väga sageli (80–99%) | Esineb 2 haiguses |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Väga sageli (80–99%) | Esineb 1 haiguses |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Väga sageli (80–99%) | Esineb 3 haiguses |
| GTF2Igeneral transcription factor IIi | Väga sageli (80–99%) | Esineb 1 haiguses |
| GTF2IRD1GTF2I repeat domain containing 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GTF2IRD2GTF2I repeat domain containing 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LIMK1LIM domain kinase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| METTL27methyltransferase like 27 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NCF1neutrophil cytosolic factor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NSD1nuclear receptor binding SET domain protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RAI1retinoic acid induced 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| RFC2replication factor C subunit 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| STX1Asyntaxin 1A | Väga sageli (80–99%) | Esineb 1 haiguses |
| SUZ12SUZ12 polycomb repressive complex 2 subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| TBL2transducin beta like 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TMEM270transmembrane protein 270 | Väga sageli (80–99%) | Esineb 1 haiguses |
| VPS37DVPS37D subunit of ESCRT-I | Väga sageli (80–99%) | Esineb 1 haiguses |
| ACANaggrecan | Sageli (30–79%) | Esineb 2 haiguses |
| AFF2ALF transcription elongation factor 2 | Sageli (30–79%) | Esineb 2 haiguses |
| AIPAHR interacting HSP90 co-chaperone | Sageli (30–79%) | Esineb 1 haiguses |
| C1Rcomplement C1r | Sageli (30–79%) | Esineb 2 haiguses |
| C1Scomplement C1s | Sageli (30–79%) | Esineb 1 haiguses |
| CDC73cell division cycle 73 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 64 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| EIF4A3eukaryotic translation initiation factor 4A3 | Sageli (30–79%) | Esineb 1 haiguses |
| GDAP1ganglioside induced differentiation associated protein 1 | Sageli (30–79%) | Esineb 3 haiguses |
| GPC4glypican 4 | Sageli (30–79%) | Esineb 2 haiguses |
| GPR101G protein-coupled receptor 101 | Sageli (30–79%) | Esineb 1 haiguses |
| IQSEC2IQ motif and Sec7 domain ArfGEF 2 | Sageli (30–79%) | Esineb 1 haiguses |
| LAMA3laminin subunit alpha 3 | Sageli (30–79%) | Esineb 2 haiguses |
| LAMB3laminin subunit beta 3 | Sageli (30–79%) | Esineb 1 haiguses |
| LAMC2laminin subunit gamma 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MATR3matrin 3 | Sageli (30–79%) | Esineb 2 haiguses |
| MLXIPLMLX interacting protein like | Sageli (30–79%) | Esineb 1 haiguses |
| MYH14myosin heavy chain 14 | Sageli (30–79%) | Esineb 2 haiguses |
| NKX2-5NK2 homeobox 5 | Sageli (30–79%) | Esineb 1 haiguses |
| PAX8paired box 8 | Sageli (30–79%) | Esineb 1 haiguses |
| TLK2tousled like kinase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TRHRthyrotropin releasing hormone receptor | Sageli (30–79%) | Esineb 1 haiguses |
| TSHBthyroid stimulating hormone subunit beta | Sageli (30–79%) | Esineb 1 haiguses |
| ACTA1actin alpha 1, skeletal muscle | Mõnikord (5–29%) | Esineb 1 haiguses |
| ADARadenosine deaminase RNA specific | Mõnikord (5–29%) | Esineb 1 haiguses |
| DDRGK1DDRGK domain containing 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| FBN1fibrillin 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| GPC3glypican 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HACD13-hydroxyacyl-CoA dehydratase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IFIH1interferon induced with helicase C domain 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ITGA7integrin subunit alpha 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LSM11LSM11, U7 small nuclear RNA associated | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAPK1mitogen-activated protein kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MFN2mitofusin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MID1midline 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MYL2myosin light chain 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NFE2L2NFE2 like bZIP transcription factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPP3CAprotein phosphatase 3 catalytic subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNASEH2Aribonuclease H2 subunit A | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNASEH2Bribonuclease H2 subunit B | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNASEH2Cribonuclease H2 subunit C | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNU7-1RNA, U7 small nuclear 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SAMHD1SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SELENONselenoprotein N | Mõnikord (5–29%) | Esineb 1 haiguses |
| SERPING1serpin family G member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SHOC2SHOC2 leucine rich repeat scaffold protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPARTspartin | Mõnikord (5–29%) | Esineb 1 haiguses |
| TPM2tropomyosin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TPM3tropomyosin 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TREX1three prime repair exonuclease 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRT16keratin 16 | Harva (1–4%) | Esineb 1 haiguses |
| KRT17keratin 17 | Harva (1–4%) | Esineb 2 haiguses |
| KRT6Akeratin 6A | Harva (1–4%) | Esineb 1 haiguses |
| KRT6Bkeratin 6B | Harva (1–4%) | Esineb 2 haiguses |
| SPTBN1spectrin beta, non-erythrocytic 1 | Harva (1–4%) | Esineb 1 haiguses |
| AGAaspartylglucosaminidase | Pole registreeritud | Esineb 1 haiguses |
| ARID1BAT-rich interaction domain 1B | Pole registreeritud | Esineb 1 haiguses |
| EDAectodysplasin A | Pole registreeritud | Esineb 1 haiguses |
| FLNAfilamin A | Pole registreeritud | Esineb 1 haiguses |
| HRASHRas proto-oncogene, GTPase | Pole registreeritud | Esineb 1 haiguses |
| IDSiduronate 2-sulfatase | Pole registreeritud | Esineb 1 haiguses |
| LEMD3LEM domain containing 3 | Pole registreeritud | Esineb 1 haiguses |
| LIFRLIF receptor subunit alpha | Pole registreeritud | Esineb 1 haiguses |
| SDHAF2succinate dehydrogenase complex assembly factor 2 | Pole registreeritud | Esineb 1 haiguses |
| SDHCsuccinate dehydrogenase complex subunit C | Pole registreeritud | Esineb 1 haiguses |
| SDHDsuccinate dehydrogenase complex subunit D | Pole registreeritud | Esineb 1 haiguses |
| SLC19A2solute carrier family 19 member 2 | Pole registreeritud | Esineb 1 haiguses |
| SLC26A2solute carrier family 26 member 2 | Pole registreeritud | Esineb 1 haiguses |
| THRAthyroid hormone receptor alpha | Pole registreeritud | Esineb 1 haiguses |
| TRPV4transient receptor potential cation channel subfamily V member 4 | 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.
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Logi sisseKüsiAlustaalates 449 $
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast