Træk
Positive regitine blocking test
A positive response to the regitine blocking test consisting of a substantial reduction in blood pressure following administration of regitine, indicative of the presence of increased levels of epinephrine and norepinephrine in the circulation, which is seen in pheochromocytoma-associated hypertension.
Resumé
- Kropssystem
- Abnormality of the cardiovascular system
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/positive-regitine-blocking-test.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Positive regitine blocking test, og resten af dit genom, med én test.
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Bestil min Genome Test16 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.
- Hereditary Pheochromocytoma and ParagangliomaReads 9 of these genesMAXRETSDHASDHAF2SDHBSDHCAbout this report →
- Urinary and Renal System TumourReads 5 of these genesRETSDHASDHAF2SDHBVHLAbout this report →
- Malignant Endocrine NeoplasmReads 4 of these genesRETSDHASDHAF2SDHBAbout this report →
- Hereditary Gastrointestinal Stromal TumourReads 2 of these genesSDHBSDHCAbout this report →
Show 12 more reports
- Hereditary Leiomyomatosis and Renal Cell CancerReads 1 of these genesFHAbout this report →
- Von Hippel-Lindau DiseaseReads 1 of these genesVHLAbout this report →
- PolycythemiaReads 2 of these genesEPAS1VHLAbout this report →
- Kidney CancerReads 2 of these genesSDHBVHLAbout this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesRETAbout this report →
- NeurofibromatosisReads 1 of these genesNF1About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesDNMT3AAbout this report →
- Thyroid CancerReads 1 of these genesRETAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesFHSDHAAbout this report →
- Leigh SyndromeReads 1 of these genesSDHAAbout this report →
- Epilepsy (Full Panel)Reads 1 of these genesMDH2About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesSDHAAbout this report →
Læs de gener, der er knyttet til Positive regitine blocking test, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test17 gener knyttet til Positive regitine blocking test
Ændringer i disse gener forårsager sjældne tilstande, hvor Positive regitine blocking test 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 |
|---|---|---|
| DLSTdihydrolipoamide S-succinyltransferase | Ofte (30–79 %) | I 1 tilstand |
| DNMT3ADNA methyltransferase 3 alpha | Ofte (30–79 %) | I 1 tilstand |
| EPAS1endothelial PAS domain protein 1 | Ofte (30–79 %) | I 1 tilstand |
| FHfumarate hydratase | Ofte (30–79 %) | I 1 tilstand |
| KIF1Bkinesin family member 1B | Ofte (30–79 %) | I 2 tilstande |
| MAXMYC associated transcriptional regulator X | Ofte (30–79 %) | I 2 tilstande |
| MDH2malate dehydrogenase 2 | Ofte (30–79 %) | I 1 tilstand |
| NF1neurofibromin 1 | Ofte (30–79 %) | I 1 tilstand |
| RETret proto-oncogene | Ofte (30–79 %) | I 3 tilstande |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Ofte (30–79 %) | I 1 tilstand |
| SDHAF2succinate dehydrogenase complex assembly factor 2 | Ofte (30–79 %) | I 1 tilstand |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Ofte (30–79 %) | I 2 tilstande |
| SDHCsuccinate dehydrogenase complex subunit C | Ofte (30–79 %) | I 1 tilstand |
| SDHDsuccinate dehydrogenase complex subunit D | Ofte (30–79 %) | I 2 tilstande |
| SLC25A11solute carrier family 25 member 11 | Ofte (30–79 %) | I 1 tilstand |
| TMEM127transmembrane protein 127 | Ofte (30–79 %) | I 2 tilstande |
| VHLvon Hippel-Lindau tumor suppressor | Ofte (30–79 %) | I 3 tilstande |
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 2026.10.19-9814e911.
From traits to your genome
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Gratis forsendelse · Resultater på 6–8 uger
