Træk
High urine cortisol level
Klinisk navn: Increased urinary cortisol level
Abnormally increased concentration of cortisol in the urine.
Resumé
Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/increased-urinary-cortisol-level.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til High urine cortisol level, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min 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 →
Læs de gener, der er knyttet til High urine cortisol level, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test16 gener knyttet til High urine cortisol level
Ændringer i disse gener forårsager sjældne tilstande, hvor High urine cortisol level ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| ARMC5armadillo repeat containing 5 | Altid | I 2 tilstande |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Altid | I 3 tilstande |
| ATRXATRX chromatin remodeler | Meget ofte (80–99 %) | I 1 tilstand |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Meget ofte (80–99 %) | I 1 tilstand |
| CDH23cadherin related 23 | Meget ofte (80–99 %) | I 1 tilstand |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Meget ofte (80–99 %) | I 2 tilstande |
| TP53tumor protein p53 | Meget ofte (80–99 %) | I 2 tilstande |
| USP48ubiquitin specific peptidase 48 | Meget ofte (80–99 %) | I 1 tilstand |
| USP8ubiquitin specific peptidase 8 | Meget ofte (80–99 %) | I 1 tilstand |
| CDKN2Acyclin dependent kinase inhibitor 2A | Ofte (30–79 %) | I 1 tilstand |
| CTNNB1catenin beta 1 | Ofte (30–79 %) | I 1 tilstand |
| GNASGNAS complex locus | Ofte (30–79 %) | I 1 tilstand |
| KDM1Alysine demethylase 1A | Ofte (30–79 %) | I 1 tilstand |
| TERTtelomerase reverse transcriptase | Ofte (30–79 %) | I 1 tilstand |
| ZNRF3zinc and ring finger 3 | Ofte (30–79 %) | I 1 tilstand |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Nogle gange (5–29 %) | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.18-8b139e39.
From traits to your genome
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Gratis forsendelse · Resultater på 6–8 uger
