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PrisijungtiKlaustiSekvenuokite savo genomą↗
Požymis
Recurrent fractures
The repeated occurrence of bone fractures (implying an abnormally increased tendency for fracture).
Santrauka
- Taip pat vadinama
- Increased fracture rate, Increased fractures, Multiple fractures, Multiple spontaneous fractures, Varying degree of multiple fractures, Frequent fractures
- Kūno sistema
- Abnormality of the musculoskeletal system
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/recurrent-fractures.json"
page <- fromJSON(url)
page$trait$nameRecurrent fracturesHP:0002757
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Recurrent fractures, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test73 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.
- Osteogenesis ImperfectaReads 25 of these genesCOL1A1CREB3L1CRTAPFKBP10IFITM5MBTPS2About this report →
- Dyskeratosis CongenitaReads 13 of these genesACDCTC1DKC1NHP2NOP10NPM1About this report →
- OsteopetrosisReads 9 of these genesPLEKHM1CLCN7OSTM1SNX10TCIRG1TNFRSF11AAbout this report →
- Hypogonadotropic HypogonadismReads 13 of these genesANOS1CHD7FEZF1FGF17FGF8FGFR1About this report →
Show 69 more reports
- Familial Paget Disease of BoneReads 3 of these genesTNFRSF11ATNFRSF11BZNF687About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 4 of these genesCYP27B1VDRCYP2R1SLC34A3About this report →
- Dent Disease and Lowe SyndromeReads 2 of these genesOCRLCLCN5About this report →
- Hereditary FibromatosesReads 2 of these genesANTXR2PDGFRBAbout this report →
- Familial Pulmonary FibrosisReads 4 of these genesPARNPOT1RTEL1TERTAbout this report →
- Ehlers-Danlos SyndromeReads 6 of these genesB3GALT6COL1A1COL1A2ADAMTS2B4GALT7PRDM5About this report →
- Monogenic Early-Onset OsteoporosisReads 2 of these genesWNT1COPB2About this report →
- Cutis LaxaReads 4 of these genesGORABPYCR1EMILIN1ATP7AAbout this report →
- Caffey DiseaseReads 1 of these genesCOL1A1About this report →
- Campomelic DysplasiaReads 1 of these genesSOX9About this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- CLCN7-Related Hypopigmentation, Organomegaly and Delayed Myelination (HOD)Reads 1 of these genesCLCN7About this report →
- DCC-Related Mirror Movements and Agenesis of the Corpus CallosumReads 1 of these genesDCCAbout this report →
- H SyndromeReads 1 of these genesSLC29A3About this report →
- Hajdu-Cheney SyndromeReads 1 of these genesNOTCH2About this report →
- HypophosphatasiaReads 1 of these genesALPLAbout this report →
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- Spondyloepiphyseal Dysplasia With Congenital Joint DislocationsReads 1 of these genesCHST3About this report →
- Stüve-Wiedemann SyndromeReads 1 of these genesLIFRAbout this report →
- VitreoretinopathyReads 4 of these genesCOL11A1CTC1LRP5FZD4About this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 2 of these genesTERCTERTAbout this report →
- Alagille SyndromeReads 1 of these genesNOTCH2About this report →
- Cleidocranial DysplasiaReads 1 of these genesRUNX2About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Hypercalcemia InfantileReads 1 of these genesSLC34A1About this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- TRIP11-Related Skeletal DysplasiaReads 1 of these genesTRIP11About this report →
- Noonan SyndromeReads 3 of these genesHRASKRASNRASAbout this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- MedulloblastomaReads 1 of these genesELP1About this report →
- Thyroid CancerReads 3 of these genesCASRTRPV6GNASAbout this report →
- Achondrogenesis panelReads 1 of these genesTRIP11About this report →
- MelanomaReads 1 of these genesPOT1About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNFIXAbout this report →
- Polycystic Liver Disease (1 and 2)Reads 1 of these genesLRP5About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesGNASAbout this report →
- Distal MyopathiesReads 2 of these genesVCPANO5About this report →
- PancreatitisReads 1 of these genesTRPV6About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesLRP5About this report →
- Autoimmune DiseaseReads 2 of these genesSTAT3KRASAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 2 of these genesNGFELP1About this report →
- Congenital Disorders of GlycosylationReads 4 of these genesB3GALT6GORABB3GAT3MOGSAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 6 of these genesVCPEMILIN1NGFATP7AELP1RRM2BAbout this report →
- Hypertrophic CardiomyopathyReads 3 of these genesHRASKRASNRASAbout this report →
- Spinal Muscular AtrophyReads 2 of these genesEMILIN1ATP7AAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Basal Ganglia CalcificationReads 1 of these genesPDGFRBAbout this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 1 of these genesCASRAbout this report →
- Waardenburg SyndromeReads 1 of these genesSOX10About this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesVCPEMILIN1ATP7AAbout this report →
- Familial HypomagnesemiaReads 1 of these genesTRPV6About this report →
- Urea Cycle DisorderReads 1 of these genesSLC7A7About this report →
- Frontotemporal DementiaReads 1 of these genesVCPAbout this report →
- Congenital HypothyroidismReads 1 of these genesFOXE1About this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesCBSAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesMINPP1About this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesHESX1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesVCPAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesANO5About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesMBTPS2About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesVCPEMILIN1ATP7AAbout this report →
- Other Inborn Errors of ImmunityReads 2 of these genesSTAT3KRASAbout this report →
- Intellectual DisabilityReads 2 of these genesSMSWDR11About this report →
- Hearing Loss and DeafnessReads 1 of these genesCOL11A1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesRRM2BAbout this report →
Vienu tyrimu sužinokite genus, susijusius su Recurrent fractures, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test138 genų susiję su Recurrent fractures
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Recurrent fractures. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| B3GALT6beta-1,3-galactosyltransferase 6 | Visada | 2 ligose |
| CCDC134coiled-coil domain containing 134 | Visada | 1 ligoje |
| COL11A1collagen type XI alpha 1 chain | Visada | 1 ligoje |
| COL1A1collagen type I alpha 1 chain | Visada | 5 ligose |
| CREB3L1cAMP responsive element binding protein 3 like 1 | Visada | 1 ligoje |
| CRTAPcartilage associated protein | Visada | 2 ligose |
| CYP27B1cytochrome P450 family 27 subfamily B member 1 | Visada | 1 ligoje |
| FKBP10FKBP prolyl isomerase 10 | Visada | 2 ligose |
| IFITM5interferon induced transmembrane protein 5 | Visada | 1 ligoje |
| IRX5iroquois homeobox 5 | Visada | 1 ligoje |
| LBRlamin B receptor | Visada | 1 ligoje |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Visada | 1 ligoje |
| MIR2861microRNA 2861 | Visada | 1 ligoje |
| P3H1prolyl 3-hydroxylase 1 | Visada | 1 ligoje |
| P4HBprolyl 4-hydroxylase subunit beta | Visada | 2 ligose |
| PLEKHM1pleckstrin homology and RUN domain containing M1 | Visada | 2 ligose |
| PPIBpeptidylprolyl isomerase B | Visada | 1 ligoje |
| SEC24DSEC24 homolog D, COPII component | Visada | 2 ligose |
| SERPINF1serpin family F member 1 | Visada | 1 ligoje |
| SLC34A1solute carrier family 34 member 1 | Visada | 1 ligoje |
| SP7Sp7 transcription factor | Visada | 1 ligoje |
| SPARCsecreted protein acidic and cysteine rich | Visada | 1 ligoje |
| TENT5Aterminal nucleotidyltransferase 5A | Visada | 1 ligoje |
| UNC45Aunc-45 myosin chaperone A | Visada | 1 ligoje |
| WNT1Wnt family member 1 | Visada | 2 ligose |
| ANTXR2ANTXR cell adhesion molecule 2 | Labai dažnai (80–99%) | 1 ligoje |
| CASRcalcium sensing receptor | Labai dažnai (80–99%) | 2 ligose |
| CBScystathionine beta-synthase | Labai dažnai (80–99%) | 1 ligoje |
| CLCN7Cl-/H+ antiporter 7 | Labai dažnai (80–99%) | 5 ligose |
| COL1A2collagen type I alpha 2 chain | Labai dažnai (80–99%) | 4 ligose |
| DKK1dickkopf Wnt signaling pathway inhibitor 1 | Labai dažnai (80–99%) | 1 ligoje |
| GORABgolgin, RAB6 interacting | Labai dažnai (80–99%) | 2 ligose |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Labai dažnai (80–99%) | 1 ligoje |
| PLOD2procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 | Labai dažnai (80–99%) | 1 ligoje |
| PYCR1pyrroline-5-carboxylate reductase 1 | Labai dažnai (80–99%) | 1 ligoje |
| SLC29A3solute carrier family 29 member 3 | Labai dažnai (80–99%) | 2 ligose |
| SNX10sorting nexin 10 | Labai dažnai (80–99%) | 1 ligoje |
| SOX9SRY-box transcription factor 9 | Labai dažnai (80–99%) | 1 ligoje |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Labai dažnai (80–99%) | 3 ligose |
| TMEM38Btransmembrane protein 38B | Labai dažnai (80–99%) | 1 ligoje |
Rodyti dar 98 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| TNFRSF11ATNF receptor superfamily member 11a | Labai dažnai (80–99%) | 2 ligose |
| TNFRSF11BTNF receptor superfamily member 11b | Labai dažnai (80–99%) | 2 ligose |
| TNFSF11TNF superfamily member 11 | Labai dažnai (80–99%) | 2 ligose |
| TRPV6transient receptor potential cation channel subfamily V member 6 | Labai dažnai (80–99%) | 2 ligose |
| VCPvalosin containing protein | Labai dažnai (80–99%) | 1 ligoje |
| VDRvitamin D receptor | Labai dažnai (80–99%) | 2 ligose |
| WNT3AWnt family member 3A | Labai dažnai (80–99%) | 1 ligoje |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Dažnai (30–79%) | 1 ligoje |
| ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2 | Dažnai (30–79%) | 1 ligoje |
| ADAMTSL2ADAMTS like 2 | Dažnai (30–79%) | 1 ligoje |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Dažnai (30–79%) | 1 ligoje |
| BMP1bone morphogenetic protein 1 | Dažnai (30–79%) | 1 ligoje |
| CA2carbonic anhydrase 2 | Dažnai (30–79%) | 1 ligoje |
| CHD6chromodomain helicase DNA binding protein 6 | Dažnai (30–79%) | 1 ligoje |
| CHST3carbohydrate sulfotransferase 3 | Dažnai (30–79%) | 1 ligoje |
| CLTCL1clathrin heavy chain like 1 | Dažnai (30–79%) | 1 ligoje |
| COPB2coat protein complex I subunit beta 2 | Dažnai (30–79%) | 1 ligoje |
| CTC1CST telomere replication complex component 1 | Dažnai (30–79%) | 1 ligoje |
| DKC1dyskerin pseudouridine synthase 1 | Dažnai (30–79%) | 1 ligoje |
| EMILIN1elastin microfibril interfacer 1 | Dažnai (30–79%) | 1 ligoje |
| GLE1GLE1 RNA export mediator | Dažnai (30–79%) | 1 ligoje |
| LIFRLIF receptor subunit alpha | Dažnai (30–79%) | 1 ligoje |
| LRP5LDL receptor related protein 5 | Dažnai (30–79%) | 2 ligose |
| LRRC8Cleucine rich repeat containing 8 VRAC subunit C | Dažnai (30–79%) | 1 ligoje |
| NGFnerve growth factor | Dažnai (30–79%) | 1 ligoje |
| NHP2NHP2 ribonucleoprotein | Dažnai (30–79%) | 1 ligoje |
| NOP10NOP10 ribonucleoprotein | Dažnai (30–79%) | 1 ligoje |
| NOTCH2notch receptor 2 | Dažnai (30–79%) | 1 ligoje |
| NPM1nucleophosmin 1 | Dažnai (30–79%) | 1 ligoje |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Dažnai (30–79%) | 1 ligoje |
| PARNpoly(A)-specific ribonuclease | Dažnai (30–79%) | 1 ligoje |
| PHLDB1pleckstrin homology like domain family B member 1 | Dažnai (30–79%) | 1 ligoje |
| POT1protection of telomeres 1 | Dažnai (30–79%) | 1 ligoje |
| RTEL1regulator of telomere elongation helicase 1 | Dažnai (30–79%) | 1 ligoje |
| SMSspermine synthase | Dažnai (30–79%) | 2 ligose |
| STAT3signal transducer and activator of transcription 3 | Dažnai (30–79%) | 2 ligose |
| TERCtelomerase RNA component | Dažnai (30–79%) | 1 ligoje |
| TERTtelomerase reverse transcriptase | Dažnai (30–79%) | 1 ligoje |
| TINF2TERF1 interacting nuclear factor 2 | Dažnai (30–79%) | 1 ligoje |
| TRIP11thyroid hormone receptor interactor 11 | Dažnai (30–79%) | 1 ligoje |
| TYMSthymidylate synthetase | Dažnai (30–79%) | 1 ligoje |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Dažnai (30–79%) | 1 ligoje |
| WRAP53WD repeat containing antisense to TP53 | Dažnai (30–79%) | 1 ligoje |
| ANO5anoctamin 5 | Kartais (5–29%) | 1 ligoje |
| ANOS1anosmin 1 | Kartais (5–29%) | 1 ligoje |
| ATP7AATPase copper transporting alpha | Kartais (5–29%) | 1 ligoje |
| B4GALT7beta-1,4-galactosyltransferase 7 | Kartais (5–29%) | 1 ligoje |
| CCDC141coiled-coil domain containing 141 | Kartais (5–29%) | 1 ligoje |
| CHD7chromodomain helicase DNA binding protein 7 | Kartais (5–29%) | 1 ligoje |
| CTNND2catenin delta 2 | Kartais (5–29%) | 1 ligoje |
| DCCDCC netrin 1 receptor | Kartais (5–29%) | 1 ligoje |
| DUSP6dual specificity phosphatase 6 | Kartais (5–29%) | 1 ligoje |
| ELP1elongator acetyltransferase complex subunit 1 | Kartais (5–29%) | 1 ligoje |
| EMX2empty spiracles homeobox 2 | Kartais (5–29%) | 1 ligoje |
| FEZF1FEZ family zinc finger 1 | Kartais (5–29%) | 1 ligoje |
| FGF17fibroblast growth factor 17 | Kartais (5–29%) | 1 ligoje |
| FGF8fibroblast growth factor 8 | Kartais (5–29%) | 1 ligoje |
| FGFR1fibroblast growth factor receptor 1 | Kartais (5–29%) | 1 ligoje |
| FLRT3fibronectin leucine rich transmembrane protein 3 | Kartais (5–29%) | 1 ligoje |
| FOXE1forkhead box E1 | Kartais (5–29%) | 1 ligoje |
| GNASGNAS complex locus | Kartais (5–29%) | 2 ligose |
| HABP2hyaluronan binding protein 2 | Kartais (5–29%) | 1 ligoje |
| HESX1HESX homeobox 1 | Kartais (5–29%) | 1 ligoje |
| HS6ST1heparan sulfate 6-O-sulfotransferase 1 | Kartais (5–29%) | 1 ligoje |
| IDH1isocitrate dehydrogenase (NADP(+)) 1 | Kartais (5–29%) | 1 ligoje |
| IDH2isocitrate dehydrogenase (NADP(+)) 2 | Kartais (5–29%) | 1 ligoje |
| IL17RDinterleukin 17 receptor D | Kartais (5–29%) | 1 ligoje |
| MINPP1multiple inositol-polyphosphate phosphatase 1 | Kartais (5–29%) | 1 ligoje |
| MYH3myosin heavy chain 3 | Kartais (5–29%) | 1 ligoje |
| NDNFneuron derived neurotrophic factor | Kartais (5–29%) | 1 ligoje |
| NFIXnuclear factor I X | Kartais (5–29%) | 1 ligoje |
| PDGFRBplatelet derived growth factor receptor beta | Kartais (5–29%) | 1 ligoje |
| PRDM5PR/SET domain 5 | Kartais (5–29%) | 1 ligoje |
| PROK2prokineticin 2 | Kartais (5–29%) | 1 ligoje |
| PROKR2prokineticin receptor 2 | Kartais (5–29%) | 1 ligoje |
| PTENphosphatase and tensin homolog | Kartais (5–29%) | 1 ligoje |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Kartais (5–29%) | 1 ligoje |
| RUNX2RUNX family transcription factor 2 | Kartais (5–29%) | 1 ligoje |
| SEMA3Asemaphorin 3A | Kartais (5–29%) | 1 ligoje |
| SEMA5Asemaphorin 5A | Kartais (5–29%) | 1 ligoje |
| SOX10SRY-box transcription factor 10 | Kartais (5–29%) | 1 ligoje |
| SPRY4sprouty RTK signaling antagonist 4 | Kartais (5–29%) | 1 ligoje |
| TACR3tachykinin receptor 3 | Kartais (5–29%) | 1 ligoje |
| WDR11WD repeat domain 11 | Kartais (5–29%) | 1 ligoje |
| ALPLalkaline phosphatase, biomineralization associated | Neužfiksuota | 1 ligoje |
| CLCN5Cl-/H+ antiporter 5 | Neužfiksuota | 2 ligose |
| CYP2R1cytochrome P450 family 2 subfamily R member 1 | Neužfiksuota | 1 ligoje |
| FZD4frizzled class receptor 4 | Neužfiksuota | 1 ligoje |
| HRASHRas proto-oncogene, GTPase | Neužfiksuota | 1 ligoje |
| KDELR2KDEL endoplasmic reticulum protein retention receptor 2 | Neužfiksuota | 1 ligoje |
| KRASKRas proto-oncogene, GTPase | Neužfiksuota | 1 ligoje |
| MOGSmannosyl-oligosaccharide glucosidase | Neužfiksuota | 1 ligoje |
| NRASNRAS proto-oncogene, GTPase | Neužfiksuota | 1 ligoje |
| SGMS2sphingomyelin synthase 2 | Neužfiksuota | 1 ligoje |
| SLC34A3solute carrier family 34 member 3 | Neužfiksuota | 1 ligoje |
| SLC7A7solute carrier family 7 member 7 | Neužfiksuota | 1 ligoje |
| YY1AP1YY1 associated protein 1 | Neužfiksuota | 1 ligoje |
| ZNF687zinc finger protein 687 | Neužfiksuota | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
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- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.19-9814e911.
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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 810+ physician-ready reports.
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