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Özellik
Double ureter
Klinik adı: Ureteral duplication
A developmental anomaly characterized by the presence of two, instead of one, ureter connecting a kidney to the bladder.
Özet
- Vücut sistemi
- Abnormality of the genitourinary system
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Bu sayfanın veri olarak görünümü
Veriyi JSON olarak okumak için sayfa adresinin sonuna .json ekleyin veya application/json isteyin.
library(jsonlite)
url <- "https://dantelabs.com/traits/ureteral-duplication.json"
page <- fromJSON(url)
page$trait$nameDouble ureterHP:0000073
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Double ureter ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi al39 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.
- Meckel SyndromeReads 9 of these genesB9D1B9D2MKS1RPGRIP1LTCTN2TMEM107About this report →
- Joubert Syndrome And Related DisordersReads 15 of these genesB9D1B9D2CC2D2ACEP290CSPP1MKS1About this report →
- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 8 of these genesCC2D2ACEP290CSPP1MKS1TMEM216TMEM231About this report →
Show 35 more reports
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Focal Dermal Hypoplasia (Goltz Syndrome)Reads 1 of these genesPORCNAbout this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- Scalp-Ear-Nipple SyndromeReads 1 of these genesKCTD1About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- Stankiewicz-Isidor SyndromeReads 1 of these genesPSMD12About this report →
- Hereditary Gingival FibromatosisReads 1 of these genesSOS1About this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 2 of these genesCEP290RPGRIP1About this report →
- Bardet-Biedl and Alström SyndromesReads 2 of these genesCEP290MKS1About this report →
- Inherited Neurodegenerative DisordersReads 8 of these genesCC2D2ACEP290CSPP1MKS1TMEM216TMEM231About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesNODALAbout this report →
- Polycystic Kidney DiseaseReads 1 of these genesIFT140About this report →
- Congenital Diarrhoeas & EnteropathiesReads 1 of these genesSPINT2About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA6About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesAPC2About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesSOS1NSD1About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesCPT2About this report →
- Retinitis PigmentosaReads 2 of these genesIFT140CC2D2AAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGNAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesGATA6About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesTMEM67About this report →
- Noonan SyndromeReads 1 of these genesSOS1About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesAPC2About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesB3GLCTPIGNAbout this report →
- Diabetes MellitusReads 1 of these genesGATA6About this report →
- Inherited ThrombocytopeniasReads 1 of these genesRBM8AAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesLMNAAbout this report →
Double ureter ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi alDouble ureter ile ilişkili 42 gen
Bu genlerdeki değişiklikler, Double ureter özelliğinin görüldüğü nadir durumlara yol açar. Bu özelliğe sahip çoğu kişide bu durumlardan hiçbiri yoktur; ayrıca bu listedeki bir gen, kimsenin kendi genomu hakkında bir şey söylemez.
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| IFT140intraflagellar transport 140 | Her zaman | 1 durumda |
| FUZfuzzy planar cell polarity protein | Sık (%30–79) | 1 durumda |
| GPC3glypican 3 | Sık (%30–79) | 1 durumda |
| GPC4glypican 4 | Sık (%30–79) | 1 durumda |
| NCAPG2non-SMC condensin II complex subunit G2 | Sık (%30–79) | 1 durumda |
| SLC6A17solute carrier family 6 member 17 | Sık (%30–79) | 2 durumda |
| VANGL1VANGL planar cell polarity protein 1 | Sık (%30–79) | 1 durumda |
| B3GLCTbeta 3-glucosyltransferase | Bazen (%5–29) | 2 durumda |
| B9D1B9 domain containing 1 | Bazen (%5–29) | 1 durumda |
| B9D2B9 domain containing 2 | Bazen (%5–29) | 1 durumda |
| CC2D2Acoiled-coil and C2 domain containing 2A | Bazen (%5–29) | 1 durumda |
| CEP290centrosomal protein 290 | Bazen (%5–29) | 1 durumda |
| CSPP1centrosome and spindle pole associated protein 1 | Bazen (%5–29) | 1 durumda |
| GATA6GATA binding protein 6 | Bazen (%5–29) | 2 durumda |
| KCTD1potassium channel tetramerization domain containing 1 | Bazen (%5–29) | 1 durumda |
| KDM6Alysine demethylase 6A | Bazen (%5–29) | 1 durumda |
| KMT2Dlysine methyltransferase 2D | Bazen (%5–29) | 1 durumda |
| LMNAlamin A/C | Bazen (%5–29) | 1 durumda |
| MKS1MKS transition zone complex subunit 1 | Bazen (%5–29) | 1 durumda |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Bazen (%5–29) | 1 durumda |
| RPGRIP1RPGR interacting protein 1 | Bazen (%5–29) | 1 durumda |
| RPGRIP1LRPGRIP1 like | Bazen (%5–29) | 1 durumda |
| SOS1SOS Ras/Rac guanine nucleotide exchange factor 1 | Bazen (%5–29) | 1 durumda |
| SPINT2serine peptidase inhibitor, Kunitz type 2 | Bazen (%5–29) | 1 durumda |
| TCTN1tectonic family member 1 | Bazen (%5–29) | 1 durumda |
| TCTN2tectonic family member 2 | Bazen (%5–29) | 1 durumda |
| TCTN3tectonic family member 3 | Bazen (%5–29) | 1 durumda |
| TMEM107transmembrane protein 107 | Bazen (%5–29) | 1 durumda |
| TMEM216transmembrane protein 216 | Bazen (%5–29) | 1 durumda |
| TMEM231transmembrane protein 231 | Bazen (%5–29) | 1 durumda |
| TMEM237transmembrane protein 237 | Bazen (%5–29) | 1 durumda |
| TMEM67transmembrane protein 67 | Bazen (%5–29) | 1 durumda |
| TXNDC15thioredoxin domain containing 15 | Bazen (%5–29) | 1 durumda |
| ZMPSTE24zinc metallopeptidase STE24 | Bazen (%5–29) | 2 durumda |
| APC2APC regulator of Wnt signaling pathway 2 | Seyrek (%1–4) | 1 durumda |
| NODALnodal growth differentiation factor | Seyrek (%1–4) | 1 durumda |
| NSD1nuclear receptor binding SET domain protein 1 | Seyrek (%1–4) | 1 durumda |
| RBM8ARNA binding motif protein 8A | Seyrek (%1–4) | 1 durumda |
| AXIN1axin 1 | Kaydedilmedi | 1 durumda |
| CPT2carnitine palmitoyltransferase 2 | Kaydedilmedi | 1 durumda |
2 gen daha göster
Bu özelliğin, genin ilişkili olduğu durumlardan birine sahip kişiler arasında ne sıklıkta görüldüğü; Human Phenotype Ontology'nin kaydettiği şekliyle, bunlar arasında en sık görülen oran. Bu sayfalar özellikleri ve bunların arkasındaki araştırmaları anlatır; tanı koymaz. Belirtiler hakkında bir doktora veya genetik danışmana başvurmanız gerekir.
Daha dar özellikler
Daha geniş özellikler
Bilgilerin kaynağı
- Human Phenotype Ontology, 2026-09-01 sürümü: özellik, adları, tanımı ve buna bağlı genler. Ayrıntılar için hpo.jax.org adresine bakın.
- Veri sürümü 2026.10.19-9814e911.
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
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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.
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