AtlasTræk
Hydrocele testis
Accumulation of clear fluid in the between the layers of membrane (tunica vaginalis) surrounding the testis.
Resumé
- Også kaldet
- Testicular hydrocele
- Kropssystem
- Abnormality of the genitourinary system
AtlasDenne 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/hydrocele-testis.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Hydrocele testis, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test26 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.
- Primary Lymphoedema & Lymphatic MalformationsReads 8 of these genesADAMTS3SOX18ANGPT2FLT4MDFICTHSD1About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 2 of these genesNSD1EZH2About this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- FLT4-Related Congenital Heart DiseaseReads 1 of these genesFLT4About this report →
Show 22 more reports
- Intracranial Berry AneurysmReads 1 of these genesTHSD1About this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Kabuki SyndromeReads 1 of these genesKMT2DAbout this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGLPIGNAbout this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Rare Inherited Bone Marrow Failure SyndromesReads 1 of these genesMECOMAbout this report →
- Congenital Disorders of GlycosylationReads 4 of these genesPIGLEDEM3MOGSPIGNAbout this report →
- Red Blood Cell Membrane DisordersReads 1 of these genesPIEZO1About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- Intellectual DisabilityReads 5 of these genesPIGLCREBBPEP300NAA10ZEB2About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX11BAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesAPC2About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesAPC2About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesZMYM2About this report →
- Inherited ThrombocytopeniasReads 1 of these genesMECOMAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesNSD1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPEX11BAbout this report →
- Epilepsy (Full Panel)Reads 1 of these genesZEB2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesTBX1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesPEX11BAbout this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesPEX11BAbout this report →
Læs de gener, der er knyttet til Hydrocele testis, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test35 gener knyttet til Hydrocele testis
Ændringer i disse gener forårsager sjældne tilstande, hvor Hydrocele testis 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 |
|---|---|---|
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Altid | I 1 tilstand |
| CIROZciliated left-right organizer protein containing ZP-N domains | Altid | I 1 tilstand |
| FRYLFRY like transcription coactivator | Altid | I 1 tilstand |
| MECOMMDS1 and EVI1 complex locus | Altid | I 1 tilstand |
| SLC25A10solute carrier family 25 member 10 | Altid | I 1 tilstand |
| SOX18SRY-box transcription factor 18 | Altid | I 3 tilstande |
| ANGPT2angiopoietin 2 | Meget ofte (80–99 %) | I 1 tilstand |
| DPH2diphthamide biosynthesis 2 | Ofte (30–79 %) | I 1 tilstand |
| FLT4fms related receptor tyrosine kinase 4 | Ofte (30–79 %) | I 2 tilstande |
| MDFICMyoD family inhibitor domain containing | Ofte (30–79 %) | I 1 tilstand |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Ofte (30–79 %) | I 1 tilstand |
| PTENphosphatase and tensin homolog | Ofte (30–79 %) | I 2 tilstande |
| SETD1ASET domain containing 1A, histone lysine methyltransferase | Ofte (30–79 %) | I 1 tilstand |
| SPECC1Lsperm antigen with calponin homology and coiled-coil domains 1 like | Ofte (30–79 %) | I 1 tilstand |
| THSD1thrombospondin type 1 domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| VEGFCvascular endothelial growth factor C | Ofte (30–79 %) | I 1 tilstand |
| ADAMTS15ADAM metallopeptidase with thrombospondin type 1 motif 15 | Nogle gange (5–29 %) | I 1 tilstand |
| CREBBPCREB binding lysine acetyltransferase | Nogle gange (5–29 %) | I 1 tilstand |
| EDEM3ER degradation enhancing alpha-mannosidase like protein 3 | Nogle gange (5–29 %) | I 1 tilstand |
| EP300EP300 lysine acetyltransferase | Nogle gange (5–29 %) | I 1 tilstand |
| FOCADfocadhesin | Nogle gange (5–29 %) | I 1 tilstand |
| KMT2Dlysine methyltransferase 2D | Nogle gange (5–29 %) | I 1 tilstand |
| MOGSmannosyl-oligosaccharide glucosidase | Nogle gange (5–29 %) | I 1 tilstand |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Nogle gange (5–29 %) | I 1 tilstand |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Nogle gange (5–29 %) | I 2 tilstande |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Nogle gange (5–29 %) | I 3 tilstande |
| TBX1T-box transcription factor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ZMYM2zinc finger MYM-type containing 2 | Nogle gange (5–29 %) | I 1 tilstand |
| APC2APC regulator of Wnt signaling pathway 2 | Sjældent (1–4%) | I 1 tilstand |
| NSD1nuclear receptor binding SET domain protein 1 | Sjældent (1–4%) | I 1 tilstand |
| ZEB2zinc finger E-box binding homeobox 2 | Sjældent (1–4%) | I 2 tilstande |
| ATAD3AATPase family AAA domain containing 3A | Ikke registreret | I 1 tilstand |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Ikke registreret | I 1 tilstand |
| PEX11Bperoxisomal biogenesis factor 11 beta | Ikke registreret | I 1 tilstand |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Ikke registreret | I 1 tilstand |
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.
Snævrere træk
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.
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