Tunnus
Blurred vision
Lack of sharpness of vision resulting in the inability to see fine detail.
Kokkuvõte
- Kehasüsteem
- Abnormality of the eye
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Blurred vision, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test56 geeni on seotud tunnusega Blurred vision
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Blurred vision. 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 |
|---|---|---|
| FDXRferredoxin reductase | Alati | Esineb 1 haiguses |
| LIM2lens intrinsic membrane protein 2 | Alati | Esineb 1 haiguses |
| SOSTsclerostin | Alati | Esineb 1 haiguses |
| UBAP1Lubiquitin associated protein 1 like | Alati | Esineb 1 haiguses |
| TACSTD2tumor associated calcium signal transducer 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ABCA1ATP binding cassette subfamily A member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| APOA1apolipoprotein A1 | Sageli (30–79%) | Esineb 1 haiguses |
| COL17A1collagen type XVII alpha 1 chain | Sageli (30–79%) | Esineb 1 haiguses |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Sageli (30–79%) | Esineb 1 haiguses |
| FASFas cell surface death receptor | Sageli (30–79%) | Esineb 1 haiguses |
| HLA-Amajor histocompatibility complex, class I, A | Sageli (30–79%) | Esineb 1 haiguses |
| HLA-Bmajor histocompatibility complex, class I, B | Sageli (30–79%) | Esineb 1 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sageli (30–79%) | Esineb 3 haiguses |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Sageli (30–79%) | Esineb 2 haiguses |
| LAMP2lysosome associated membrane protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MAPTmicrotubule associated protein tau | Sageli (30–79%) | Esineb 2 haiguses |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Sageli (30–79%) | Esineb 1 haiguses |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Sageli (30–79%) | Esineb 1 haiguses |
| MT-CYBmitochondrially encoded cytochrome b | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND4Lmitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Sageli (30–79%) | Esineb 1 haiguses |
| NDUFS2NADH:ubiquinone oxidoreductase core subunit S2 | Sageli (30–79%) | Esineb 1 haiguses |
| NOP56NOP56 ribonucleoprotein | Sageli (30–79%) | Esineb 1 haiguses |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Sageli (30–79%) | Esineb 2 haiguses |
| SLC4A11solute carrier family 4 member 11 | Sageli (30–79%) | Esineb 1 haiguses |
| ALMS1ALMS1 centrosome and basal body associated protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| CABP4calcium binding protein 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DBHdopamine beta-hydroxylase | Mõnikord (5–29%) | Esineb 1 haiguses |
| HGSNATheparan-alpha-glucosaminide N-acetyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNJ13potassium inwardly rectifying channel subfamily J member 13 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LCA5lebercilin LCA5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LRATlecithin retinol acyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| OTX2orthodenticle homeobox 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRPH2peripherin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
Näita veel 16 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| RPE65retinoid isomerohydrolase RPE65 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPATA7spermatogenesis associated 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TGFBItransforming growth factor beta induced | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRANK1tetratricopeptide repeat and ankyrin repeat containing 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Harva (1–4%) | Esineb 1 haiguses |
| COL8A2collagen type VIII alpha 2 chain | Harva (1–4%) | Esineb 1 haiguses |
| GRHL2grainyhead like transcription factor 2 | Harva (1–4%) | Esineb 1 haiguses |
| OVOL2ovo like zinc finger 2 | Harva (1–4%) | Esineb 1 haiguses |
| SLC12A3solute carrier family 12 member 3 | Harva (1–4%) | Esineb 2 haiguses |
| VSX1visual system homeobox 1 | Harva (1–4%) | Esineb 1 haiguses |
| ZEB1zinc finger E-box binding homeobox 1 | Harva (1–4%) | Esineb 1 haiguses |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Pole registreeritud | Esineb 1 haiguses |
| COL4A1collagen type IV alpha 1 chain | Pole registreeritud | Esineb 1 haiguses |
| NLRP3NLR family pyrin domain containing 3 | Pole registreeritud | Esineb 1 haiguses |
| SCN9Asodium voltage-gated channel alpha subunit 9 | 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