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Egenskap
Hydroureter
The distention of the ureter with urine.
Sammanfattning
- Även kallad
- Dilated ureter, Megaureter, Swelling of ureter, Ureteral dilatation, Wide ureter
- Kroppssystem
- Abnormality of the genitourinary system
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Den här sidan som data
Lägg till .json i sidans adress, eller begär application/json, för att läsa den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/hydroureter.json"
page <- fromJSON(url)
page$trait$nameHydroureterHP:0000072
AtlasVem vi hjälperVår vetenskapProdukterResultat
Logga inFrågaSekvensera ditt genom↗
Läs generna kopplade till Hydroureter, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test50 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.
- Fanconi AnemiaReads 18 of these genesBRCA1BRCA2BRIP1ERCC4FANCAFANCBAbout this report →
- DNA Repair DiseaseReads 20 of these genesBRCA1BRCA2BRIP1ERCC4ERCC6ERCC8About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 4 of these genesACTG2MYH11MYLKFLNAAbout this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
Show 46 more reports
- Nephrogenic Diabetes InsipidusReads 2 of these genesAQP2AVPR2About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesBRIP1PALB2RAD51CAbout this report →
- Alveolar Capillary Dysplasia with Misalignment of Pulmonary VeinsReads 1 of these genesFOXF1About this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- PLD1-Related Congenital Heart DiseaseReads 1 of these genesPLD1About this report →
- Raine SyndromeReads 1 of these genesFAM20CAbout this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 2 of these genesEVCEVC2About this report →
- Wolfram Syndrome & WFS1 SpectrumReads 1 of these genesWFS1About this report →
- Epidermolysis BullosaReads 3 of these genesLAMA3LAMB3LAMC2About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 2 of these genesSOX17TBX18About this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRNU4ATACAbout this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesRIPK4About this report →
- Aortic AneurysmReads 2 of these genesMYH11MYLKAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGTPIGNAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Bardet-Biedl and Alström SyndromesReads 2 of these genesBBS12MKKSAbout this report →
- Lissencephaly Spectrum DisordersReads 2 of these genesACTBACTG1About this report →
- Cornelia de Lange SyndromeReads 1 of these genesSMC3About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- Intellectual DisabilityReads 5 of these genesTAF4NAA10ARID1BMED12SETBP1About this report →
- Coffin-Siris SyndromeReads 1 of these genesARID1BAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Female InfertilityReads 2 of these genesFANCMTP63About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesNSD1SOS2About this report →
- Amelogenesis ImperfectaReads 1 of these genesLAMB3About this report →
- Ectodermal DysplasiasReads 1 of these genesTP63About this report →
- Noonan SyndromeReads 1 of these genesSOS2About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesWFS1About this report →
- Syndromic CraniosynostosisReads 1 of these genesRAB23About this report →
- Hearing Loss and DeafnessReads 2 of these genesACTG1WFS1About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesPIGTPIGNAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesGLI3About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesACTBAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesMBTPS2About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesMBTPS2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesACTBAbout this report →
- Male InfertilityReads 1 of these genesFANCMAbout this report →
- Primary Mitochondrial DiseaseReads 1 of these genesNDUFAF3About this report →
- Epilepsy (Full Panel)Reads 1 of these genesFLNAAbout this report →
Läs generna kopplade till Hydroureter, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test79 gener kopplade till Hydroureter
Förändringar i dessa gener orsakar sällsynta tillstånd där Hydroureter förekommer. De flesta med denna egenskap har inget av dessa tillstånd, och en gen på listan säger ingenting om någons eget genom.
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| LMOD1leiomodin 1 | Alltid | I 2 tillstånd |
| TAF4TATA-box binding protein associated factor 4 | Alltid | I 1 tillstånd |
| ACTG2actin gamma 2, smooth muscle | Mycket ofta (80–99 %) | I 3 tillstånd |
| CHRM3cholinergic receptor muscarinic 3 | Mycket ofta (80–99 %) | I 2 tillstånd |
| RNU4ATACRNA, U4atac small nuclear | Mycket ofta (80–99 %) | I 1 tillstånd |
| ACTBactin beta | Ofta (30–79 %) | I 1 tillstånd |
| ACTG1actin gamma 1 | Ofta (30–79 %) | I 1 tillstånd |
| BBS12Bardet-Biedl syndrome 12 | Ofta (30–79 %) | I 1 tillstånd |
| BCORBCL6 corepressor | Ofta (30–79 %) | I 2 tillstånd |
| GPC3glypican 3 | Ofta (30–79 %) | I 1 tillstånd |
| GPC4glypican 4 | Ofta (30–79 %) | I 1 tillstånd |
| MYH11myosin heavy chain 11 | Ofta (30–79 %) | I 1 tillstånd |
| MYLKmyosin light chain kinase | Ofta (30–79 %) | I 2 tillstånd |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Ofta (30–79 %) | I 2 tillstånd |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Ofta (30–79 %) | I 1 tillstånd |
| RIPK4receptor interacting serine/threonine kinase 4 | Ofta (30–79 %) | I 1 tillstånd |
| AQP2aquaporin 2 | Ibland (5–29 %) | I 1 tillstånd |
| ARID1BAT-rich interaction domain 1B | Ibland (5–29 %) | I 1 tillstånd |
| AVPR2arginine vasopressin receptor 2 | Ibland (5–29 %) | I 1 tillstånd |
| BRCA1BRCA1 DNA repair associated | Ibland (5–29 %) | I 1 tillstånd |
| BRCA2BRCA2 DNA repair associated | Ibland (5–29 %) | I 1 tillstånd |
| BRIP1BRCA1 interacting DNA helicase 1 | Ibland (5–29 %) | I 1 tillstånd |
| CCNQcyclin Q | Ibland (5–29 %) | I 1 tillstånd |
| DDB1damage specific DNA binding protein 1 | Ibland (5–29 %) | I 1 tillstånd |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Ibland (5–29 %) | I 1 tillstånd |
| EDNRAendothelin receptor type A | Ibland (5–29 %) | I 1 tillstånd |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Ibland (5–29 %) | I 1 tillstånd |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Ibland (5–29 %) | I 1 tillstånd |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Ibland (5–29 %) | I 1 tillstånd |
| EVCEvC ciliary complex subunit 1 | Ibland (5–29 %) | I 1 tillstånd |
| EVC2EvC ciliary complex subunit 2 | Ibland (5–29 %) | I 1 tillstånd |
| FAAP100FA core complex associated protein 100 | Ibland (5–29 %) | I 1 tillstånd |
| FAM20CFAM20C golgi associated secretory pathway kinase | Ibland (5–29 %) | I 1 tillstånd |
| FANCAFA complementation group A | Ibland (5–29 %) | I 1 tillstånd |
| FANCBFA complementation group B | Ibland (5–29 %) | I 1 tillstånd |
| FANCCFA complementation group C | Ibland (5–29 %) | I 1 tillstånd |
| FANCD2FA complementation group D2 | Ibland (5–29 %) | I 1 tillstånd |
| FANCEFA complementation group E | Ibland (5–29 %) | I 1 tillstånd |
| FANCFFA complementation group F | Ibland (5–29 %) | I 1 tillstånd |
| FANCGFA complementation group G | Ibland (5–29 %) | I 1 tillstånd |
Visa 39 gener till
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| FANCIFA complementation group I | Ibland (5–29 %) | I 1 tillstånd |
| FANCLFA complementation group L | Ibland (5–29 %) | I 1 tillstånd |
| FANCMFA complementation group M | Ibland (5–29 %) | I 1 tillstånd |
| FOXF1forkhead box F1 | Ibland (5–29 %) | I 1 tillstånd |
| GLI1GLI family zinc finger 1 | Ibland (5–29 %) | I 1 tillstånd |
| HS2ST1heparan sulfate 2-O-sulfotransferase 1 | Ibland (5–29 %) | I 1 tillstånd |
| LAMA3laminin subunit alpha 3 | Ibland (5–29 %) | I 1 tillstånd |
| LAMB3laminin subunit beta 3 | Ibland (5–29 %) | I 1 tillstånd |
| LAMC2laminin subunit gamma 2 | Ibland (5–29 %) | I 1 tillstånd |
| LONP1lon peptidase 1, mitochondrial | Ibland (5–29 %) | I 1 tillstånd |
| MAD2L2mitotic arrest deficient 2 like 2 | Ibland (5–29 %) | I 1 tillstånd |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Ibland (5–29 %) | I 1 tillstånd |
| MED12mediator complex subunit 12 | Ibland (5–29 %) | I 1 tillstånd |
| NDUFAF3NADH:ubiquinone oxidoreductase complex assembly factor 3 | Ibland (5–29 %) | I 1 tillstånd |
| NSD1nuclear receptor binding SET domain protein 1 | Ibland (5–29 %) | I 1 tillstånd |
| PALB2partner and localizer of BRCA2 | Ibland (5–29 %) | I 1 tillstånd |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Ibland (5–29 %) | I 1 tillstånd |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Ibland (5–29 %) | I 1 tillstånd |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Ibland (5–29 %) | I 1 tillstånd |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Ibland (5–29 %) | I 1 tillstånd |
| RAD51RAD51 recombinase | Ibland (5–29 %) | I 1 tillstånd |
| RAD51CRAD51 paralog C | Ibland (5–29 %) | I 1 tillstånd |
| RFWD3ring finger and WD repeat domain 3 | Ibland (5–29 %) | I 1 tillstånd |
| SLX4SLX4 structure-specific endonuclease subunit | Ibland (5–29 %) | I 1 tillstånd |
| SMC3structural maintenance of chromosomes 3 | Ibland (5–29 %) | I 1 tillstånd |
| SOS2SOS Ras/Rho guanine nucleotide exchange factor 2 | Ibland (5–29 %) | I 1 tillstånd |
| SOX17SRY-box transcription factor 17 | Ibland (5–29 %) | I 1 tillstånd |
| TBX18T-box transcription factor 18 | Ibland (5–29 %) | I 1 tillstånd |
| UBE2Tubiquitin conjugating enzyme E2 T | Ibland (5–29 %) | I 1 tillstånd |
| XRCC2X-ray repair cross complementing 2 | Ibland (5–29 %) | I 1 tillstånd |
| FLNAfilamin A | Inte registrerat | I 1 tillstånd |
| GLI3GLI family zinc finger 3 | Inte registrerat | I 1 tillstånd |
| HPSE2heparanase 2 (inactive) | Inte registrerat | I 1 tillstånd |
| MKKSMKKS centrosomal shuttling protein | Inte registrerat | I 1 tillstånd |
| PLD1phospholipase D1 | Inte registrerat | I 1 tillstånd |
| RAB23RAB23, member RAS oncogene family | Inte registrerat | I 1 tillstånd |
| SETBP1SET binding protein 1 | Inte registrerat | I 1 tillstånd |
| TP63tumor protein p63 | Inte registrerat | I 1 tillstånd |
| WFS1wolframin ER transmembrane glycoprotein | Inte registrerat | I 1 tillstånd |
Hur ofta det förekommer hos personer med ett av genens tillstånd, den vanligaste frekvensen bland dem, enligt Human Phenotype Ontology. Dessa sidor beskriver egenskaper och forskningen bakom dem. De är inte en diagnos, och det är läkare eller genetisk rådgivare du bör fråga om symtom.
Mer specifika egenskaper
Bredare egenskaper
Varifrån informationen kommer
- Human Phenotype Ontology, version 2026-09-01: egenskapen, dess namn, definition och de gener som är kopplade till den. Läs mer på hpo.jax.org.
- Dataversion 2026.10.19-9814e911.
AtlasVem vi hjälperVår vetenskapProdukterResultat
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From traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
Från 449 $
Fri frakt · Resultat inom 6–8 veckor
