Tunnus
High urine cortisol level
Kliiniline nimetus: Increased urinary cortisol level
Abnormally increased concentration of cortisol in the urine.
Kokkuvõte
Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/increased-urinary-cortisol-level.json"
page <- fromJSON(url)
page$trait$nameLugege välja geenid, mis on seotud High urine cortisol level-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test22 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 2 of these genesARMC5PRKAR1AAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 2 of these genesPRKAR1AGNASAbout this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- KDM1A-Related Neurodevelopmental DisorderReads 1 of these genesKDM1AAbout this report →
Show 18 more reports
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- Malignant Endocrine NeoplasmReads 2 of these genesTP53CDKN1BAbout this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- MelanomaReads 1 of these genesCDKN2AAbout this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesTERTAbout this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR3C1About this report →
- Familial Pulmonary FibrosisReads 1 of these genesTERTAbout this report →
- Kidney CancerReads 1 of these genesTP53About this report →
- Usher SyndromeReads 1 of these genesCDH23About this report →
- Urinary and Renal System TumourReads 1 of these genesTP53About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Noonan SyndromeReads 1 of these genesBRAFAbout this report →
- Dyskeratosis CongenitaReads 1 of these genesTERTAbout this report →
- Hearing Loss and DeafnessReads 2 of these genesCDH23USP48About this report →
- VitreoretinopathyReads 1 of these genesCTNNB1About this report →
- Thyroid CancerReads 1 of these genesGNASAbout this report →
- Intellectual DisabilityReads 2 of these genesATRXCTNNB1About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesBRAFAbout this report →
Lugege välja geenid, mis on seotud High urine cortisol level-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test16 geeni on seotud tunnusega High urine cortisol level
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb High urine cortisol level. 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 |
|---|---|---|
| ARMC5armadillo repeat containing 5 | Alati | Esineb 2 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Alati | Esineb 3 haiguses |
| ATRXATRX chromatin remodeler | Väga sageli (80–99%) | Esineb 1 haiguses |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| CDH23cadherin related 23 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TP53tumor protein p53 | Väga sageli (80–99%) | Esineb 2 haiguses |
| USP48ubiquitin specific peptidase 48 | Väga sageli (80–99%) | Esineb 1 haiguses |
| USP8ubiquitin specific peptidase 8 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CDKN2Acyclin dependent kinase inhibitor 2A | Sageli (30–79%) | Esineb 1 haiguses |
| CTNNB1catenin beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GNASGNAS complex locus | Sageli (30–79%) | Esineb 1 haiguses |
| KDM1Alysine demethylase 1A | Sageli (30–79%) | Esineb 1 haiguses |
| TERTtelomerase reverse transcriptase | Sageli (30–79%) | Esineb 1 haiguses |
| ZNRF3zinc and ring finger 3 | Sageli (30–79%) | Esineb 1 haiguses |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Mõnikord (5–29%) | 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 2026.10.19-9814e911.
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Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
