Tunnus
Prolonged prothrombin time
Increased time to coagulation in the prothrombin time test, which is a measure of the extrinsic pathway of coagulation. The results of the prothrombin time test are often expressed in terms of the International normalized ratio (INR), which is calculated as a ratio of the patient's prothrombin time (PT) to a control PT standardized for the potency of the thromboplastin reagent developed by the World Health Organization (WHO) using the formula: INR is equal to Patient PT divided by Control PT.
Kokkuvõte
- Teised nimetused
- Increased INR, Increased international normalised ratio, Increased international normalized ratio, Low factor II activity, Prolonged PT, Reduced factor II activity, Reduced prothrombin activity
Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/prolonged-prothrombin-time.json"
page <- fromJSON(url)
page$trait$nameLugege välja geenid, mis on seotud Prolonged prothrombin time-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test53 geeni on seotud tunnusega Prolonged prothrombin time
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Prolonged prothrombin time. 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 |
|---|---|---|
| AMACRalpha-methylacyl-CoA racemase | Alati | Esineb 1 haiguses |
| CYP7B1cytochrome P450 family 7 subfamily B member 1 | Alati | Esineb 1 haiguses |
| EFL1elongation factor like GTPase 1 | Alati | Esineb 1 haiguses |
| F10coagulation factor X | Alati | Esineb 2 haiguses |
| GGCXgamma-glutamyl carboxylase | Alati | Esineb 3 haiguses |
| MICOS13mitochondrial contact site and cristae organizing system subunit 13 | Alati | Esineb 1 haiguses |
| NR1H4nuclear receptor subfamily 1 group H member 4 | Alati | Esineb 1 haiguses |
| PET100PET100 cytochrome c oxidase chaperone | Alati | Esineb 1 haiguses |
| PSMB9proteasome 20S subunit beta 9 | Alati | Esineb 1 haiguses |
| RINT1RAD50 interactor 1 | Alati | Esineb 1 haiguses |
| RNU6ATACRNA, U6atac small nuclear | Alati | Esineb 1 haiguses |
| SLC37A4solute carrier family 37 member 4 | Alati | Esineb 1 haiguses |
| SOS2SOS Ras/Rho guanine nucleotide exchange factor 2 | Alati | Esineb 1 haiguses |
| TRMUtRNA mitochondrial 2-thiouridylase | Alati | Esineb 1 haiguses |
| ADKadenosine kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| F2coagulation factor II, thrombin | Väga sageli (80–99%) | Esineb 2 haiguses |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| LMAN1lectin, mannose binding 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MCFD2multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| MPV17mitochondrial inner membrane protein MPV17 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC25A13solute carrier family 25 member 13 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ACAD9acyl-CoA dehydrogenase family member 9 | Sageli (30–79%) | Esineb 1 haiguses |
| AHCYadenosylhomocysteinase | Sageli (30–79%) | Esineb 1 haiguses |
| AKR1D1aldo-keto reductase family 1 member D1 | Sageli (30–79%) | Esineb 1 haiguses |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| ANO6anoctamin 6 | Sageli (30–79%) | Esineb 1 haiguses |
| CD46CD46 molecule | Sageli (30–79%) | Esineb 1 haiguses |
| CFHcomplement factor H | Sageli (30–79%) | Esineb 1 haiguses |
| CFIcomplement factor I | Sageli (30–79%) | Esineb 1 haiguses |
| F7coagulation factor VII | Sageli (30–79%) | Esineb 1 haiguses |
| HELLPARHELLP associated long non-coding RNA | Sageli (30–79%) | Esineb 1 haiguses |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Sageli (30–79%) | Esineb 1 haiguses |
| PGM1phosphoglucomutase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| VKORC1vitamin K epoxide reductase complex subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CLPBClpB family mitochondrial disaggregase | Mõnikord (5–29%) | Esineb 1 haiguses |
| COG8component of oligomeric golgi complex 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| F8coagulation factor VIII | Mõnikord (5–29%) | Esineb 1 haiguses |
| GPR35G protein-coupled receptor 35 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HADHhydroxyacyl-CoA dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| MST1macrophage stimulating 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
Näita veel 13 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| MTTPmicrosomal triglyceride transfer protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| NGLY1N-glycanase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| OTCornithine transcarbamylase | Mõnikord (5–29%) | Esineb 1 haiguses |
| SEMA4Dsemaphorin 4D | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC30A10solute carrier family 30 member 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TCF4transcription factor 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| F5coagulation factor V | Pole registreeritud | Esineb 1 haiguses |
| FAHfumarylacetoacetate hydrolase | Pole registreeritud | Esineb 1 haiguses |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Pole registreeritud | Esineb 1 haiguses |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Pole registreeritud | Esineb 1 haiguses |
| NBASNBAS subunit of NRZ tethering complex | Pole registreeritud | Esineb 1 haiguses |
| PMM2phosphomannomutase 2 | Pole registreeritud | Esineb 1 haiguses |
| PRF1perforin 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 2026.10.17-8666dff2.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast