Tunnus
Double vision
Kliiniline nimetus: Diplopia
Diplopia is a condition in which a single object is perceived as two images, it is also known as double vision.
Kokkuvõte
- Kehasüsteem
- Abnormality of the eye
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Double vision, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test78 geeni on seotud tunnusega Double vision
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Double 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 |
|---|---|---|
| ABCB1ATP binding cassette subfamily B member 1 | Alati | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Alati | Esineb 3 haiguses |
| RAB3ARAB3A, member RAS oncogene family | Alati | Esineb 1 haiguses |
| RFC4replication factor C subunit 4 | Alati | Esineb 1 haiguses |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Alati | Esineb 1 haiguses |
| TOP3ADNA topoisomerase III alpha | Alati | Esineb 1 haiguses |
| TYMPthymidine phosphorylase | Alati | Esineb 1 haiguses |
| MYO5Amyosin VA | Väga sageli (80–99%) | Esineb 1 haiguses |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Sageli (30–79%) | Esineb 2 haiguses |
| ATXN3ataxin 3 | Sageli (30–79%) | Esineb 4 haiguses |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Sageli (30–79%) | Esineb 4 haiguses |
| DNAJC13DnaJ heat shock protein family (Hsp40) member C13 | Sageli (30–79%) | Esineb 1 haiguses |
| EIF4G1eukaryotic translation initiation factor 4 gamma 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Sageli (30–79%) | Esineb 1 haiguses |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Sageli (30–79%) | Esineb 1 haiguses |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Sageli (30–79%) | Esineb 1 haiguses |
| ERCC5ERCC excision repair 5, endonuclease | Sageli (30–79%) | Esineb 1 haiguses |
| FGF14fibroblast growth factor 14 | Sageli (30–79%) | Esineb 1 haiguses |
| GBA1glucosylceramidase beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GIGYF2GRB10 interacting GYF protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| LRRK2leucine rich repeat kinase 2 | Sageli (30–79%) | Esineb 2 haiguses |
| PRRT2proline rich transmembrane protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| RILPL1Rab interacting lysosomal protein like 1 | Sageli (30–79%) | Esineb 1 haiguses |
| RTN2reticulon 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SAMD9Lsterile alpha motif domain containing 9 like | Sageli (30–79%) | Esineb 1 haiguses |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC2A1solute carrier family 2 member 1 | Sageli (30–79%) | Esineb 2 haiguses |
| SNCAsynuclein alpha | Sageli (30–79%) | Esineb 2 haiguses |
| TPP1tripeptidyl peptidase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| VPS35VPS35 retromer complex component | Sageli (30–79%) | Esineb 1 haiguses |
| ADPRSADP-ribosylserine hydrolase | Mõnikord (5–29%) | Esineb 1 haiguses |
| AIPAHR interacting HSP90 co-chaperone | Mõnikord (5–29%) | Esineb 1 haiguses |
| ANO10anoctamin 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Mõnikord (5–29%) | Esineb 2 haiguses |
| CDH23cadherin related 23 | Mõnikord (5–29%) | Esineb 2 haiguses |
| DKK1dickkopf Wnt signaling pathway inhibitor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-Bmajor histocompatibility complex, class I, B | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| KCND3potassium voltage-gated channel subfamily D member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
Näita veel 38 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| MEN1menin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Mõnikord (5–29%) | Esineb 2 haiguses |
| NFKB2nuclear factor kappa B subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPTX1neuronal pentraxin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRNPprion protein (Kanno blood group) | Mõnikord (5–29%) | Esineb 2 haiguses |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC1A3solute carrier family 1 member 3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SPTBN2spectrin beta, non-erythrocytic 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TMEM240transmembrane protein 240 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TTC19tetratricopeptide repeat domain 19 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TTRtransthyretin | Mõnikord (5–29%) | Esineb 1 haiguses |
| DARS2aspartyl-tRNA synthetase 2, mitochondrial | Harva (1–4%) | Esineb 1 haiguses |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Harva (1–4%) | Esineb 1 haiguses |
| GRK1G protein-coupled receptor kinase 1 | Harva (1–4%) | Esineb 1 haiguses |
| HTRA2HtrA serine peptidase 2 | Harva (1–4%) | Esineb 1 haiguses |
| NAB2NGFI-A binding protein 2 | Harva (1–4%) | Esineb 1 haiguses |
| NOP56NOP56 ribonucleoprotein | Harva (1–4%) | Esineb 1 haiguses |
| PARK7Parkinsonism associated deglycase | Harva (1–4%) | Esineb 1 haiguses |
| PINK1PTEN induced kinase 1 | Harva (1–4%) | Esineb 1 haiguses |
| PODXLpodocalyxin like | Harva (1–4%) | Esineb 1 haiguses |
| PRKNparkin RBR E3 ubiquitin protein ligase | Harva (1–4%) | Esineb 1 haiguses |
| SAGS-antigen visual arrestin | Harva (1–4%) | Esineb 1 haiguses |
| STAT6signal transducer and activator of transcription 6 | Harva (1–4%) | Esineb 1 haiguses |
| SYNJ1synaptojanin 1 | Harva (1–4%) | Esineb 1 haiguses |
| UCHL1ubiquitin C-terminal hydrolase L1 | Harva (1–4%) | Esineb 1 haiguses |
| VPS13Cvacuolar protein sorting 13 homolog C | Harva (1–4%) | Esineb 1 haiguses |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Pole registreeritud | Esineb 1 haiguses |
| MAPTmicrotubule associated protein tau | Pole registreeritud | Esineb 1 haiguses |
| MGME1mitochondrial genome maintenance exonuclease 1 | Pole registreeritud | Esineb 1 haiguses |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Pole registreeritud | Esineb 1 haiguses |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Pole registreeritud | Esineb 1 haiguses |
| MT-TNmitochondrially encoded tRNA-Asn (AAU/C) | Pole registreeritud | Esineb 1 haiguses |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Pole registreeritud | Esineb 1 haiguses |
| SERPINI1serpin family I member 1 | Pole registreeritud | Esineb 1 haiguses |
| TGFB1transforming growth factor beta 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.
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