AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Özellik
Thick eyebrow
Increased density/number and/or increased diameter of eyebrow hairs.
Özet
- Diğer adları
- Bushy eyebrows, Dense eyebrow, Heavy eyebrows, Prominent eyebrows, Thick eyebrows, Hypertrichosis of the eyebrow
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
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/thick-eyebrow.json"
page <- fromJSON(url)
page$trait$nameThick eyebrowHP:0000574
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Thick eyebrow ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi al48 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.
- Cornelia de Lange SyndromeReads 6 of these genesNIPBLBRD4HDAC8RAD21SMC1ASMC3About this report →
- Intellectual DisabilityReads 35 of these genesLAS1LSMARCB1TAF4TBL1XR1VPS13BARID1AAbout this report →
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 3 of these genesSMARCB1SMARCA4SMARCE1About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 2 of these genesKIFBPRETAbout this report →
Show 44 more reports
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 2 of these genesDNMT3ANFIXAbout this report →
- Hajdu-Cheney SyndromeReads 1 of these genesNOTCH2About this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- Mucopolysaccharidosis Type VII (Sly Syndrome)Reads 1 of these genesGUSBAbout this report →
- Epilepsy (Full Panel)Reads 11 of these genesDENND5ADEPDC5FLNASLC35A2SMC1AATP6V1B2About this report →
- Lysosomal Storage DiseaseReads 6 of these genesIDUAGNSGUSBSUMF1FUCA1MAN2B1About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 2 of these genesFUCA1MAN2B1About this report →
- Alagille SyndromeReads 1 of these genesNOTCH2About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Hereditary Multiple OsteochondromasReads 1 of these genesEXT1About this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Müllerian Aplasia (MRKH Syndrome)Reads 1 of these genesWNT4About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesHMGA2MAGEL2About this report →
- Inherited Congenital Heart DefectsReads 2 of these genesFLNATFAP2BAbout this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Mucopolysaccharidosis Type III (Sanfilippo Syndrome)Reads 1 of these genesGNSAbout this report →
- NeurofibromatosisReads 1 of these genesSMARCB1About this report →
- Female InfertilityReads 3 of these genesTP63FOXL2WNT4About this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesIGF1RAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesSIM1About this report →
- Waardenburg SyndromeReads 1 of these genesPAX3About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesRETAbout this report →
- Osteogenesis ImperfectaReads 2 of these genesNBASCOL1A2About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesRETAbout this report →
- Congenital Disorders of GlycosylationReads 3 of these genesSLC35A2B3GAT3MGAT2About this report →
- Urinary and Renal System TumourReads 1 of these genesRETAbout this report →
- Dilated CardiomyopathyReads 2 of these genesABCC9FHL1About this report →
- Leigh SyndromeReads 2 of these genesFBXL4AIFM1About this report →
- Ectodermal DysplasiasReads 1 of these genesTP63About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesACER3MTHFSAbout this report →
- Ehlers-Danlos SyndromeReads 1 of these genesCOL1A2About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesAIFM1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesCDONAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Thyroid CancerReads 1 of these genesRETAbout this report →
- Primary Mitochondrial DiseaseReads 2 of these genesFBXL4AIFM1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesTAF1About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesMAGEL2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesCWF19L1About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesERLIN2About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesAIFM1About this report →
- Hearing Loss and DeafnessReads 1 of these genesAIFM1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesNBASAbout this report →
Thick eyebrow ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi alThick eyebrow ile ilişkili 170 gen
Bu genlerdeki değişiklikler, Thick eyebrow 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 |
|---|---|---|
| ACER3alkaline ceramidase 3 | Her zaman | 1 durumda |
| AFF4ALF transcription elongation factor 4 | Her zaman | 2 durumda |
| CDH11cadherin 11 | Her zaman | 2 durumda |
| CHASERRCHD2 adjacent suppressive regulatory RNA | Her zaman | 1 durumda |
| CWF19L1CWF19 like cell cycle control factor 1 | Her zaman | 1 durumda |
| DDX59DEAD-box helicase 59 | Her zaman | 1 durumda |
| DENND5ADENN domain containing 5A | Her zaman | 1 durumda |
| DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit | Her zaman | 1 durumda |
| FLNAfilamin A | Her zaman | 1 durumda |
| JKAMPJNK1/MAPK8 associated membrane protein | Her zaman | 1 durumda |
| KCNK4potassium two pore domain channel subfamily K member 4 | Her zaman | 1 durumda |
| KNL1kinetochore scaffold 1 | Her zaman | 1 durumda |
| LAS1LLAS1 like ribosome biogenesis factor | Her zaman | 2 durumda |
| MN1MN1 proto-oncogene, transcriptional regulator | Her zaman | 1 durumda |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Her zaman | 1 durumda |
| NAV3neuron navigator 3 | Her zaman | 1 durumda |
| NIPBLNIPBL cohesin loading factor | Her zaman | 2 durumda |
| NOTCH2notch receptor 2 | Her zaman | 2 durumda |
| PAN2poly(A) specific ribonuclease subunit PAN2 | Her zaman | 1 durumda |
| PDCD6IPprogrammed cell death 6 interacting protein | Her zaman | 1 durumda |
| POLR1ARNA polymerase I subunit A | Her zaman | 1 durumda |
| PRKG2protein kinase cGMP-dependent 2 | Her zaman | 1 durumda |
| PSMC1proteasome 26S subunit, ATPase 1 | Her zaman | 1 durumda |
| SLC35A2solute carrier family 35 member A2 | Her zaman | 1 durumda |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Her zaman | 2 durumda |
| TAF4TATA-box binding protein associated factor 4 | Her zaman | 1 durumda |
| TASP1taspase 1 | Her zaman | 1 durumda |
| TBL1XR1TBL1X/Y related 1 | Her zaman | 1 durumda |
| TMCO1transmembrane and coiled-coil domains 1 | Her zaman | 2 durumda |
| VPS13Bvacuolar protein sorting 13 homolog B | Her zaman | 2 durumda |
| ABCC9ATP binding cassette subfamily C member 9 | Çok sık (%80–99) | 1 durumda |
| ARID1AAT-rich interaction domain 1A | Çok sık (%80–99) | 2 durumda |
| ARID1BAT-rich interaction domain 1B | Çok sık (%80–99) | 2 durumda |
| ARID2AT-rich interaction domain 2 | Çok sık (%80–99) | 2 durumda |
| BRD4bromodomain containing 4 | Çok sık (%80–99) | 1 durumda |
| CCDC8coiled-coil domain containing 8 subunit of 3M complex | Çok sık (%80–99) | 1 durumda |
| CUL7cullin 7 | Çok sık (%80–99) | 2 durumda |
| DPF2double PHD fingers 2 | Çok sık (%80–99) | 2 durumda |
| HDAC8histone deacetylase 8 | Çok sık (%80–99) | 2 durumda |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Çok sık (%80–99) | 2 durumda |
130 gen daha göster
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| IDUAalpha-L-iduronidase | Çok sık (%80–99) | 1 durumda |
| KCNJ8potassium inwardly rectifying channel subfamily J member 8 | Çok sık (%80–99) | 1 durumda |
| KMT2Alysine methyltransferase 2A | Çok sık (%80–99) | 2 durumda |
| MAU2MAU2 sister chromatid cohesion factor | Çok sık (%80–99) | 2 durumda |
| OBSL1obscurin like cytoskeletal adaptor 1 | Çok sık (%80–99) | 1 durumda |
| PAX3paired box 3 | Çok sık (%80–99) | 3 durumda |
| RAD21RAD21 cohesin complex component | Çok sık (%80–99) | 3 durumda |
| SLC25A24solute carrier family 25 member 24 | Çok sık (%80–99) | 1 durumda |
| SLC9A6solute carrier family 9 member A6 | Çok sık (%80–99) | 2 durumda |
| SMARCA4SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 | Çok sık (%80–99) | 2 durumda |
| SMARCC2SWI/SNF related BAF chromatin remodeling complex subunit C2 | Çok sık (%80–99) | 2 durumda |
| SMARCD1SWI/SNF related BAF chromatin remodeling complex subunit D1 | Çok sık (%80–99) | 1 durumda |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Çok sık (%80–99) | 2 durumda |
| SMC1Astructural maintenance of chromosomes 1A | Çok sık (%80–99) | 2 durumda |
| SMC3structural maintenance of chromosomes 3 | Çok sık (%80–99) | 2 durumda |
| SOX11SRY-box transcription factor 11 | Çok sık (%80–99) | 1 durumda |
| SOX4SRY-box transcription factor 4 | Çok sık (%80–99) | 1 durumda |
| SPECC1Lsperm antigen with calponin homology and coiled-coil domains 1 like | Çok sık (%80–99) | 1 durumda |
| TP63tumor protein p63 | Çok sık (%80–99) | 1 durumda |
| ANKRD11ankyrin repeat domain 11 | Sık (%30–79) | 2 durumda |
| ASCC3activating signal cointegrator 1 complex subunit 3 | Sık (%30–79) | 1 durumda |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Sık (%30–79) | 2 durumda |
| AUTS2activator of transcription and developmental regulator AUTS2 | Sık (%30–79) | 1 durumda |
| BCAS3BCAS3 microtubule associated cell migration factor | Sık (%30–79) | 1 durumda |
| BORCS8BLOC-1 related complex subunit 8 | Sık (%30–79) | 1 durumda |
| BPTFbromodomain PHD finger transcription factor | Sık (%30–79) | 1 durumda |
| CACHD1cache domain containing 1 | Sık (%30–79) | 1 durumda |
| CHD1chromodomain helicase DNA binding protein 1 | Sık (%30–79) | 1 durumda |
| CNOT2CCR4-NOT transcription complex subunit 2 | Sık (%30–79) | 1 durumda |
| CPLX1complexin 1 | Sık (%30–79) | 1 durumda |
| CTCFCCCTC-binding factor | Sık (%30–79) | 2 durumda |
| DOCK7dedicator of cytokinesis 7 | Sık (%30–79) | 2 durumda |
| DYMdymeclin | Sık (%30–79) | 1 durumda |
| EP300EP300 lysine acetyltransferase | Sık (%30–79) | 2 durumda |
| EXT1exostosin glycosyltransferase 1 | Sık (%30–79) | 1 durumda |
| FHL1four and a half LIM domains 1 | Sık (%30–79) | 1 durumda |
| FREM1FRAS1 related extracellular matrix 1 | Sık (%30–79) | 1 durumda |
| FRMD4AFERM domain containing 4A | Sık (%30–79) | 2 durumda |
| GNSglucosamine (N-acetyl)-6-sulfatase | Sık (%30–79) | 1 durumda |
| GON4Lgon-4 like | Sık (%30–79) | 1 durumda |
| GPRASP2G protein-coupled receptor associated sorting protein 2 | Sık (%30–79) | 1 durumda |
| GUSBglucuronidase beta | Sık (%30–79) | 1 durumda |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Sık (%30–79) | 3 durumda |
| KCNN3potassium calcium-activated channel subfamily N member 3 | Sık (%30–79) | 2 durumda |
| MTHFSmethenyltetrahydrofolate synthetase | Sık (%30–79) | 1 durumda |
| NBASNBAS subunit of NRZ tethering complex | Sık (%30–79) | 1 durumda |
| PHF6PHD finger protein 6 | Sık (%30–79) | 1 durumda |
| PPP1R21protein phosphatase 1 regulatory subunit 21 | Sık (%30–79) | 1 durumda |
| PRR12proline rich 12 | Sık (%30–79) | 1 durumda |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Sık (%30–79) | 1 durumda |
| RALGAPA1Ral GTPase activating protein catalytic subunit alpha 1 | Sık (%30–79) | 1 durumda |
| RPS23ribosomal protein S23 | Sık (%30–79) | 1 durumda |
| RUSC2RUN and SH3 domain containing 2 | Sık (%30–79) | 1 durumda |
| SETD1BSET domain containing 1B, histone lysine methyltransferase | Sık (%30–79) | 1 durumda |
| SHANK3SH3 and multiple ankyrin repeat domains 3 | Sık (%30–79) | 1 durumda |
| SLC6A17solute carrier family 6 member 17 | Sık (%30–79) | 2 durumda |
| SUMF1sulfatase modifying factor 1 | Sık (%30–79) | 1 durumda |
| TAF6TATA-box binding protein associated factor 6 | Sık (%30–79) | 1 durumda |
| TRPS1transcriptional repressor GATA binding 1 | Sık (%30–79) | 1 durumda |
| TUBGCP2tubulin gamma complex component 2 | Sık (%30–79) | 1 durumda |
| ABCA5ATP binding cassette subfamily A member 5 | Bazen (%5–29) | 1 durumda |
| ASXL3ASXL transcriptional regulator 3 | Bazen (%5–29) | 1 durumda |
| BICRABRD4 interacting chromatin remodeling complex associated protein | Bazen (%5–29) | 1 durumda |
| CDK13cyclin dependent kinase 13 | Bazen (%5–29) | 1 durumda |
| CHMP1Acharged multivesicular body protein 1A | Bazen (%5–29) | 1 durumda |
| CLCN3Cl-/H+ antiporter 3 | Bazen (%5–29) | 1 durumda |
| COL1A2collagen type I alpha 2 chain | Bazen (%5–29) | 1 durumda |
| CREBBPCREB binding lysine acetyltransferase | Bazen (%5–29) | 2 durumda |
| DDB1damage specific DNA binding protein 1 | Bazen (%5–29) | 1 durumda |
| DNMT3ADNA methyltransferase 3 alpha | Bazen (%5–29) | 2 durumda |
| EBF3EBF transcription factor 3 | Bazen (%5–29) | 1 durumda |
| ERLIN2ER lipid raft associated 2 | Bazen (%5–29) | 2 durumda |
| FBXL4F-box and leucine rich repeat protein 4 | Bazen (%5–29) | 1 durumda |
| FBXO31F-box protein 31 | Bazen (%5–29) | 1 durumda |
| FOXL2forkhead box L2 | Bazen (%5–29) | 1 durumda |
| GNB2G protein subunit beta 2 | Bazen (%5–29) | 1 durumda |
| GTF3C3general transcription factor IIIC subunit 3 | Bazen (%5–29) | 1 durumda |
| H4C5H4 clustered histone 5 | Bazen (%5–29) | 1 durumda |
| HIVEP2HIVEP zinc finger 2 | Bazen (%5–29) | 1 durumda |
| HMGA2high mobility group AT-hook 2 | Bazen (%5–29) | 1 durumda |
| IGF1Rinsulin like growth factor 1 receptor | Bazen (%5–29) | 1 durumda |
| JARID2jumonji and AT-rich interaction domain containing 2 | Bazen (%5–29) | 1 durumda |
| KDM5Clysine demethylase 5C | Bazen (%5–29) | 1 durumda |
| LEMD3LEM domain containing 3 | Bazen (%5–29) | 1 durumda |
| MEF2Cmyocyte enhancer factor 2C | Bazen (%5–29) | 1 durumda |
| NOTCH3notch receptor 3 | Bazen (%5–29) | 1 durumda |
| NRCAMneuronal cell adhesion molecule | Bazen (%5–29) | 1 durumda |
| PUF60poly(U) binding splicing factor 60 | Bazen (%5–29) | 1 durumda |
| RBM10RNA binding motif protein 10 | Bazen (%5–29) | 1 durumda |
| RHOBTB2Rho related BTB domain containing 2 | Bazen (%5–29) | 1 durumda |
| RNU2-2RNA, U2 small nuclear 2 | Bazen (%5–29) | 1 durumda |
| SATB1SATB homeobox 1 | Bazen (%5–29) | 1 durumda |
| SEPHS1selenophosphate synthetase 1 | Bazen (%5–29) | 1 durumda |
| SIM1SIM bHLH transcription factor 1 | Bazen (%5–29) | 1 durumda |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Bazen (%5–29) | 1 durumda |
| SOX6SRY-box transcription factor 6 | Bazen (%5–29) | 1 durumda |
| SPENspen family transcriptional repressor | Bazen (%5–29) | 1 durumda |
| TAF1TATA-box binding protein associated factor 1 | Bazen (%5–29) | 1 durumda |
| TBCKTBC1 domain containing kinase | Bazen (%5–29) | 1 durumda |
| TRIOtrio Rho guanine nucleotide exchange factor | Bazen (%5–29) | 1 durumda |
| UBR7ubiquitin protein ligase E3 component n-recognin 7 | Bazen (%5–29) | 1 durumda |
| WACWW domain containing adaptor with coiled-coil | Bazen (%5–29) | 2 durumda |
| WDR83OSWD repeat domain 83 opposite strand | Bazen (%5–29) | 1 durumda |
| WNT4Wnt family member 4 | Bazen (%5–29) | 1 durumda |
| ZFXzinc finger protein X-linked | Bazen (%5–29) | 1 durumda |
| ZSWIM6zinc finger SWIM-type containing 6 | Bazen (%5–29) | 1 durumda |
| PTBP1polypyrimidine tract binding protein 1 | Seyrek (%1–4) | 1 durumda |
| SPTBN1spectrin beta, non-erythrocytic 1 | Seyrek (%1–4) | 1 durumda |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Kaydedilmedi | 1 durumda |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Kaydedilmedi | 1 durumda |
| BCORBCL6 corepressor | Kaydedilmedi | 1 durumda |
| CDONcell adhesion associated, oncogene regulated | Kaydedilmedi | 1 durumda |
| CHST3carbohydrate sulfotransferase 3 | Kaydedilmedi | 1 durumda |
| FUCA1alpha-L-fucosidase 1 | Kaydedilmedi | 1 durumda |
| HECW2HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 | Kaydedilmedi | 1 durumda |
| KIFBPkinesin family binding protein | Kaydedilmedi | 1 durumda |
| KMT2Clysine methyltransferase 2C | Kaydedilmedi | 1 durumda |
| MAGEL2MAGE family member L2 | Kaydedilmedi | 1 durumda |
| MAN2B1mannosidase alpha class 2B member 1 | Kaydedilmedi | 1 durumda |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Kaydedilmedi | 1 durumda |
| MBD5methyl-CpG binding domain protein 5 | Kaydedilmedi | 1 durumda |
| MGAT2alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Kaydedilmedi | 1 durumda |
| NFIXnuclear factor I X | Kaydedilmedi | 1 durumda |
| NSUN2NOP2/Sun RNA methyltransferase 2 | Kaydedilmedi | 1 durumda |
| PHIPPHIP subunit of CUL4-Ring ligase complex | Kaydedilmedi | 1 durumda |
| RETret proto-oncogene | Kaydedilmedi | 1 durumda |
| RNF125ring finger protein 125 | Kaydedilmedi | 1 durumda |
| RPS6KA3ribosomal protein S6 kinase A3 | Kaydedilmedi | 1 durumda |
| SMAD4SMAD family member 4 | Kaydedilmedi | 1 durumda |
| TFAP2Btranscription factor AP-2 beta | 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 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 2026.10.17-8666dff2.
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
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 470+ physician-ready reports.
$449'den başlayan
Ücretsiz kargo · Sonuçlar 6–8 hafta içinde
