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Egenskap
Lack of bladder control due to nervous system injury
Klinisk navn: Neurogenic bladder
A type of bladder dysfunction caused by neurologic damage. Neurogenic bladder can be flaccid or spastic. Common manifestatios of neurogenic bladder are overflow incontinence, frequency, urgency, urge incontinence, and retention.
Sammendrag
- Kroppssystem
- Abnormality of the genitourinary system
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Denne siden som data
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library(jsonlite)
url <- "https://dantelabs.com/traits/neurogenic-bladder.json"
page <- fromJSON(url)
page$trait$nameHvem vi hjelperVår vitenskapProdukterResultater
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Les genene knyttet til Lack of bladder control due to nervous system injury, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test47 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.
- Bardet-Biedl and Alström SyndromesReads 22 of these genesARL6BBIP1BBS1BBS10BBS12BBS2About this report →
- Wolfram Syndrome & WFS1 SpectrumReads 2 of these genesCISD2WFS1About this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Hand-Foot-Genital SyndromeReads 1 of these genesHOXA13About this report →
Show 43 more reports
- VPS11-Related LeukodystrophyReads 1 of these genesVPS11About this report →
- Inherited Neurodegenerative DisordersReads 15 of these genesACER3FLVCR1HSPB8PEX3ATP13A2CLCN6About this report →
- Parkinson DiseaseReads 3 of these genesATP13A2FBXO7SNCAAbout this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Retinitis PigmentosaReads 6 of these genesFLVCR1ARL6BBS2CFAP418IFT172TTC8About this report →
- Neuronal Ceroid LipofuscinosisReads 2 of these genesATP13A2CLCN6About this report →
- Joubert Syndrome And Related DisordersReads 3 of these genesCEP290MKS1NPHP1About this report →
- Other Inherited LeukodystrophiesReads 4 of these genesACER3PEX3VPS11PLP1About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 2 of these genesNPHP1SDCCAG8About this report →
- Lissencephaly Spectrum DisordersReads 2 of these genesCEP85LMACF1About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 2 of these genesVPS11PLP1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 3 of these genesFLVCR1CEP290MKS1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 6 of these genesHSPB8PEX3LIG3MTFMTCHCHD10FARS2About this report →
- Spinal Muscular AtrophyReads 2 of these genesHSPB8CHCHD10About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesCEP19About this report →
- Hereditary Spastic ParaplegiaReads 3 of these genesATP13A2FARS2PLP1About this report →
- Hepatic Porphyria DisordersReads 1 of these genesPPOXAbout this report →
- PorphyriaReads 1 of these genesPPOXAbout this report →
- Meckel SyndromeReads 1 of these genesMKS1About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesATP13A2About this report →
- DNA Repair DiseaseReads 2 of these genesERCC6ERCC8About this report →
- Congenital Disorders of GlycosylationReads 3 of these genesHES7COG5COG7About this report →
- Hermansky-Pudlak SyndromeReads 1 of these genesHPS6About this report →
- Frontotemporal DementiaReads 1 of these genesCHCHD10About this report →
- Myofibrillar MyopathiesReads 1 of these genesHSPB8About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX3About this report →
- Glycogen Storage DiseaseReads 1 of these genesGBE1About this report →
- Primary Mitochondrial DiseaseReads 3 of these genesLIG3MTFMTFARS2About this report →
- Leigh SyndromeReads 2 of these genesMTFMTFARS2About this report →
- Neonatal Diabetes MellitusReads 1 of these genesMNX1About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 1 of these genesCEP290About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesWFS1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesTBCKAbout this report →
- Intellectual DisabilityReads 3 of these genesKDM6BGNB1SCAPERAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesCHCHD10About this report →
- Diabetes MellitusReads 1 of these genesMNX1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTRIM32About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesGJA1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesATXN3About this report →
- Lysosomal Storage DiseaseReads 1 of these genesCLCN6About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesHSPB8About this report →
- Hearing Loss and DeafnessReads 1 of these genesWFS1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesGNB1About this report →
Les genene knyttet til Lack of bladder control due to nervous system injury, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test69 gener knyttet til Lack of bladder control due to nervous system injury
Endringer i disse genene forårsaker sjeldne tilstander der Lack of bladder control due to nervous system injury forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ACER3alkaline ceramidase 3 | Alltid | I 1 tilstand |
| ARNT2aryl hydrocarbon receptor nuclear translocator 2 | Alltid | I 1 tilstand |
| EN1engrailed homeobox 1 | Alltid | I 1 tilstand |
| FLVCR1FLVCR choline and heme transporter 1 | Alltid | I 1 tilstand |
| HES7hes family bHLH transcription factor 7 | Alltid | I 1 tilstand |
| HOXA13homeobox A13 | Alltid | I 1 tilstand |
| HSPB8heat shock protein family B (small) member 8 | Alltid | I 1 tilstand |
| KDM6Blysine demethylase 6B | Alltid | I 1 tilstand |
| PEX3peroxisomal biogenesis factor 3 | Alltid | I 1 tilstand |
| GBE11,4-alpha-glucan branching enzyme 1 | Svært ofte (80–99 %) | I 2 tilstander |
| ATP13A2ATPase cation transporting 13A2 | Ofte (30–79 %) | I 1 tilstand |
| CHRNA3cholinergic receptor nicotinic alpha 3 subunit | Ofte (30–79 %) | I 1 tilstand |
| CLCN6Cl-/H+ antiporter 6 | Ofte (30–79 %) | I 1 tilstand |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Ofte (30–79 %) | I 1 tilstand |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Ofte (30–79 %) | I 1 tilstand |
| FBXO7F-box protein 7 | Ofte (30–79 %) | I 1 tilstand |
| GJA1gap junction protein alpha 1 | Ofte (30–79 %) | I 2 tilstander |
| LIG3DNA ligase 3 | Ofte (30–79 %) | I 1 tilstand |
| MARS2methionyl-tRNA synthetase 2, mitochondrial | Ofte (30–79 %) | I 1 tilstand |
| MTFMTmitochondrial methionyl-tRNA formyltransferase | Ofte (30–79 %) | I 1 tilstand |
| SNCAsynuclein alpha | Ofte (30–79 %) | I 1 tilstand |
| TRAPPC12trafficking protein particle complex subunit 12 | Ofte (30–79 %) | I 2 tilstander |
| VPS11VPS11 core subunit of CORVET and HOPS complexes | Ofte (30–79 %) | I 2 tilstander |
| ARL6ARF like GTPase 6 | Noen ganger (5–29 %) | I 1 tilstand |
| ATXN3ataxin 3 | Noen ganger (5–29 %) | I 3 tilstander |
| BBIP1BBSome interacting protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| BBS1Bardet-Biedl syndrome 1 | Noen ganger (5–29 %) | I 1 tilstand |
| BBS10Bardet-Biedl syndrome 10 | Noen ganger (5–29 %) | I 1 tilstand |
| BBS12Bardet-Biedl syndrome 12 | Noen ganger (5–29 %) | I 1 tilstand |
| BBS2Bardet-Biedl syndrome 2 | Noen ganger (5–29 %) | I 1 tilstand |
| BBS4Bardet-Biedl syndrome 4 | Noen ganger (5–29 %) | I 1 tilstand |
| BBS5Bardet-Biedl syndrome 5 | Noen ganger (5–29 %) | I 1 tilstand |
| BBS7Bardet-Biedl syndrome 7 | Noen ganger (5–29 %) | I 1 tilstand |
| BBS9Bardet-Biedl syndrome 9 | Noen ganger (5–29 %) | I 1 tilstand |
| CEP19centrosomal protein 19 | Noen ganger (5–29 %) | I 1 tilstand |
| CEP290centrosomal protein 290 | Noen ganger (5–29 %) | I 1 tilstand |
| CEP85Lcentrosomal protein 85L | Noen ganger (5–29 %) | I 1 tilstand |
| CFAP418cilia and flagella associated protein 418 | Noen ganger (5–29 %) | I 1 tilstand |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Noen ganger (5–29 %) | I 1 tilstand |
| COG5component of oligomeric golgi complex 5 | Noen ganger (5–29 %) | I 2 tilstander |
Vis 29 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| FARS2phenylalanyl-tRNA synthetase 2, mitochondrial | Noen ganger (5–29 %) | I 1 tilstand |
| GNB1G protein subunit beta 1 | Noen ganger (5–29 %) | I 1 tilstand |
| HPS6HPS6 biogenesis of lysosomal organelles complex 2 subunit 3 | Noen ganger (5–29 %) | I 1 tilstand |
| IFT172intraflagellar transport 172 | Noen ganger (5–29 %) | I 1 tilstand |
| IFT27intraflagellar transport 27 | Noen ganger (5–29 %) | I 1 tilstand |
| IFT74intraflagellar transport 74 | Noen ganger (5–29 %) | I 1 tilstand |
| LZTFL1leucine zipper transcription factor like 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MACF1microtubule actin crosslinking factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Noen ganger (5–29 %) | I 1 tilstand |
| MKKSMKKS centrosomal shuttling protein | Noen ganger (5–29 %) | I 1 tilstand |
| MKS1MKS transition zone complex subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MNX1motor neuron and pancreas homeobox 1 | Noen ganger (5–29 %) | I 2 tilstander |
| NOTCH3notch receptor 3 | Noen ganger (5–29 %) | I 1 tilstand |
| NPHP1nephrocystin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PLP1proteolipid protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PPOXprotoporphyrinogen oxidase | Noen ganger (5–29 %) | I 1 tilstand |
| SCAPERS-phase cyclin A associated protein in the ER | Noen ganger (5–29 %) | I 1 tilstand |
| SCLT1sodium channel and clathrin linker 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Noen ganger (5–29 %) | I 1 tilstand |
| TRIM32tripartite motif containing 32 | Noen ganger (5–29 %) | I 1 tilstand |
| TTC8tetratricopeptide repeat domain 8 | Noen ganger (5–29 %) | I 1 tilstand |
| WDPCPWD repeat containing planar cell polarity effector | Noen ganger (5–29 %) | I 1 tilstand |
| TBCDtubulin folding cofactor D | Sjelden (1–4%) | I 1 tilstand |
| TBCKTBC1 domain containing kinase | Sjelden (1–4%) | I 1 tilstand |
| CISD2CDGSH iron sulfur domain 2 | Ikke registrert | I 1 tilstand |
| COG7component of oligomeric golgi complex 7 | Ikke registrert | I 1 tilstand |
| ELOVL1ELOVL fatty acid elongase 1 | Ikke registrert | I 1 tilstand |
| VANGL1VANGL planar cell polarity protein 1 | Ikke registrert | I 1 tilstand |
| WFS1wolframin ER transmembrane glycoprotein | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.18-8b139e39.
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