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Özellik
Loss of bowel control
Klinik adı: Bowel incontinence
Involuntary fecal soiling in adults and children who have usually already been toilet trained.
Özet
- Diğer adları
- Anal incontinence, Faecal incontinence, Fecal incontinence
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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/bowel-incontinence.json"
page <- fromJSON(url)
page$trait$nameLoss of bowel controlHP:0002607
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Loss of bowel control ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi al44 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.
- Metachromatic LeukodystrophyReads 2 of these genesARSAPSAPAbout this report →
- Hereditary Spastic ParaplegiaReads 9 of these genesABCD1DSTYKPLP1ATP13A2DDHD2FA2HAbout this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- Christianson SyndromeReads 1 of these genesSLC9A6About this report →
Show 40 more reports
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- Townes-Brocks SyndromeReads 1 of these genesSALL1About this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Inherited Neurodegenerative DisordersReads 17 of these genesABCD1DSTYKPLP1SLC44A1ARSAATP13A2About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesHTRA1About this report →
- Congenital Disaccharidase DeficienciesReads 1 of these genesSIAbout this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- Other Inherited LeukodystrophiesReads 4 of these genesABCD1PLP1ARSAPSAPAbout this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesATP13A2About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesDSTYKAbout this report →
- Hermansky-Pudlak SyndromeReads 1 of these genesHPS6About this report →
- Frontotemporal DementiaReads 1 of these genesVCPAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesKYAbout this report →
- Female InfertilityReads 2 of these genesFMR1TP63About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesATP13A2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesARSAPSAPRTN2VCPAbout this report →
- Lysosomal Storage DiseaseReads 2 of these genesARSAPSAPAbout this report →
- Parkinson DiseaseReads 1 of these genesATP13A2About this report →
- Ectodermal DysplasiasReads 1 of these genesTP63About this report →
- Distal MyopathiesReads 1 of these genesVCPAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesRTN2VCPAbout this report →
- Noonan SyndromeReads 1 of these genesMAPK1About this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR3About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPLP1About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesSCN4AAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesVCPAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesGP1BBAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesNOP56About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSCN4AAbout this report →
- Male InfertilityReads 1 of these genesCFAP43About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesFLVCR1About this report →
- Intellectual DisabilityReads 2 of these genesZEB2JMJD1CAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesMAPK1About this report →
- Retinitis PigmentosaReads 1 of these genesFLVCR1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesZEB2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesTBX1About this report →
Loss of bowel control ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi alLoss of bowel control ile ilişkili 47 gen
Bu genlerdeki değişiklikler, Loss of bowel control 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 |
|---|---|---|
| HTRA1HtrA serine peptidase 1 | Her zaman | 1 durumda |
| KYkyphoscoliosis peptidase | Her zaman | 1 durumda |
| FUZfuzzy planar cell polarity protein | Çok sık (%80–99) | 1 durumda |
| VANGL1VANGL planar cell polarity protein 1 | Çok sık (%80–99) | 1 durumda |
| ABCD1ATP binding cassette subfamily D member 1 | Sık (%30–79) | 2 durumda |
| DSTYKdual serine/threonine and tyrosine protein kinase | Sık (%30–79) | 1 durumda |
| PLP1proteolipid protein 1 | Sık (%30–79) | 1 durumda |
| SLC44A1solute carrier family 44 member 1 | Sık (%30–79) | 1 durumda |
| ZEB2zinc finger E-box binding homeobox 2 | Sık (%30–79) | 2 durumda |
| ARSAarylsulfatase A | Bazen (%5–29) | 1 durumda |
| ARVCFARVCF delta catenin family member | Bazen (%5–29) | 1 durumda |
| ATP13A2ATPase cation transporting 13A2 | Bazen (%5–29) | 1 durumda |
| BCRBCR activator of RhoGEF and GTPase | Bazen (%5–29) | 1 durumda |
| COMTcatechol-O-methyltransferase | Bazen (%5–29) | 1 durumda |
| CRKLCRK like proto-oncogene, adaptor protein | Bazen (%5–29) | 1 durumda |
| DACT1dishevelled binding antagonist of beta catenin 1 | Bazen (%5–29) | 1 durumda |
| DDHD2DDHD domain containing 2 | Bazen (%5–29) | 1 durumda |
| EIF2AK2eukaryotic translation initiation factor 2 alpha kinase 2 | Bazen (%5–29) | 1 durumda |
| FA2Hfatty acid 2-hydroxylase | Bazen (%5–29) | 1 durumda |
| FGFR3fibroblast growth factor receptor 3 | Bazen (%5–29) | 1 durumda |
| FMR1fragile X messenger ribonucleoprotein 1 | Bazen (%5–29) | 2 durumda |
| GP1BBglycoprotein Ib platelet subunit beta | Bazen (%5–29) | 1 durumda |
| HIRAhistone cell cycle regulator | Bazen (%5–29) | 1 durumda |
| HPS6HPS6 biogenesis of lysosomal organelles complex 2 subunit 3 | Bazen (%5–29) | 1 durumda |
| HPSE2heparanase 2 (inactive) | Bazen (%5–29) | 1 durumda |
| ISL1ISL LIM homeobox 1 | Bazen (%5–29) | 1 durumda |
| JMJD1Cjumonji domain containing 1C | Bazen (%5–29) | 1 durumda |
| LRIG2leucine rich repeats and immunoglobulin like domains 2 | Bazen (%5–29) | 1 durumda |
| MAPK1mitogen-activated protein kinase 1 | Bazen (%5–29) | 1 durumda |
| PSAPprosaposin | Bazen (%5–29) | 1 durumda |
| RREB1ras responsive element binding protein 1 | Bazen (%5–29) | 1 durumda |
| RTN2reticulon 2 | Bazen (%5–29) | 1 durumda |
| SALL1spalt like transcription factor 1 | Bazen (%5–29) | 1 durumda |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Bazen (%5–29) | 1 durumda |
| SEC24CSEC24 homolog C, COPII component | Bazen (%5–29) | 1 durumda |
| SIsucrase-isomaltase | Bazen (%5–29) | 1 durumda |
| TBCDtubulin folding cofactor D | Bazen (%5–29) | 2 durumda |
| TBX1T-box transcription factor 1 | Bazen (%5–29) | 1 durumda |
| TP63tumor protein p63 | Bazen (%5–29) | 1 durumda |
| UBAP1ubiquitin associated protein 1 | Bazen (%5–29) | 1 durumda |
7 gen daha göster
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Bazen (%5–29) | 1 durumda |
| VCPvalosin containing protein | Bazen (%5–29) | 1 durumda |
| FLVCR1FLVCR choline and heme transporter 1 | Seyrek (%1–4) | 1 durumda |
| NOP56NOP56 ribonucleoprotein | Seyrek (%1–4) | 1 durumda |
| CFAP43cilia and flagella associated protein 43 | Kaydedilmedi | 1 durumda |
| SLC9A6solute carrier family 9 member A6 | Kaydedilmedi | 1 durumda |
| ZFYVE26zinc finger FYVE-type containing 26 | Kaydedilmedi | 1 durumda |
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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