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Özellik
Increased bone mineral density
An abnormal increase of bone mineral density, that is, of the amount of matter per cubic centimeter of bones which is often referred to as osteosclerosis. Osteosclerosis can be detected on radiological examination as an increased whiteness (density) of affected bones.
Özet
- Diğer adları
- Increased bone density, Osteosclerosis, Osteosclerosis of bones
- Vücut sistemi
- Abnormality of the musculoskeletal system
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Veriyi JSON olarak okumak için sayfa adresinin sonuna .json ekleyin veya application/json isteyin.
library(jsonlite)
url <- "https://dantelabs.com/traits/increased-bone-mineral-density.json"
page <- fromJSON(url)
page$trait$nameIncreased bone mineral densityHP:0011001
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Increased bone mineral density ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
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Genome Test'imi al60 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.
- OsteopetrosisReads 7 of these genesCLCN7OSTM1TCIRG1AMER1CTSKLRP5About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 3 of these genesLRP5SOSTTGFB1About this report →
- Familial Paget Disease of BoneReads 2 of these genesTNFRSF11ATNFRSF11BAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 2 of these genesGNASSTX16About this report →
Show 56 more reports
- Cenani-Lenz Syndactyly SyndromeReads 1 of these genesLRP4About this report →
- CLCN7-Related Hypopigmentation, Organomegaly and Delayed Myelination (HOD)Reads 1 of these genesCLCN7About this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- DesmosterolosisReads 1 of these genesDHCR24About this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- FAM111A-Related Skeletal DysplasiaReads 1 of these genesFAM111AAbout this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Ghosal Haematodiaphyseal DysplasiaReads 1 of these genesTBXAS1About this report →
- H SyndromeReads 1 of these genesSLC29A3About this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- Raine SyndromeReads 1 of these genesFAM20CAbout this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- Werner SyndromeReads 1 of these genesWRNAbout this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 2 of these genesDMP1ENPP1About this report →
- Cleidocranial DysplasiaReads 1 of these genesRUNX2About this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Hereditary Arterial CalcificationReads 1 of these genesENPP1About this report →
- Primary HyperoxaluriaReads 1 of these genesAGXTAbout this report →
- Inherited Congenital Heart DefectsReads 2 of these genesFLNAELNAbout this report →
- Achondrogenesis panelReads 1 of these genesSLC26A2About this report →
- MelanomaReads 1 of these genesMITFAbout this report →
- Polycystic Liver Disease (1 and 2)Reads 1 of these genesLRP5About this report →
- DNA Repair DiseaseReads 3 of these genesERCC2ERCC3GTF2H5About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Hereditary SpherocytosisReads 1 of these genesSLC4A2About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesTGFB1About this report →
- VitreoretinopathyReads 2 of these genesCTNNB1LRP5About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesMC4RAbout this report →
- Waardenburg SyndromeReads 1 of these genesMITFAbout this report →
- Thyroid CancerReads 2 of these genesGNASSTX16About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 2 of these genesLRP5BMP1About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesSLC26A2About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Lysosomal Storage DiseaseReads 2 of these genesCTSKGBA1About this report →
- Parkinson DiseaseReads 1 of these genesGBA1About this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- Amelogenesis ImperfectaReads 1 of these genesDLX3About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesAARS1LMNAAbout this report →
- Noonan SyndromeReads 1 of these genesMAP2K1About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesLRP4About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesERCC2About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesLPIN2About this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Epilepsy (Full Panel)Reads 2 of these genesFLNAAARS1About this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesAARS1LMNAAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesMAP2K1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesAARS1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesDNAJC30About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesNCF1About this report →
- Intellectual DisabilityReads 1 of these genesCTNNB1About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesAARS1About this report →
Increased bone mineral density ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi alIncreased bone mineral density ile ilişkili 69 gen
Bu genlerdeki değişiklikler, Increased bone mineral density 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 |
|---|---|---|
| AXIN1axin 1 | Her zaman | 1 durumda |
| CLCN7Cl-/H+ antiporter 7 | Her zaman | 1 durumda |
| FAM20CFAM20C golgi associated secretory pathway kinase | Her zaman | 1 durumda |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Her zaman | 1 durumda |
| SLC4A2solute carrier family 4 member 2 | Her zaman | 1 durumda |
| TBXAS1thromboxane A synthase 1 | Her zaman | 1 durumda |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Her zaman | 2 durumda |
| AMER1APC membrane recruitment protein 1 | Çok sık (%80–99) | 1 durumda |
| CTNNB1catenin beta 1 | Çok sık (%80–99) | 1 durumda |
| CTSKcathepsin K | Çok sık (%80–99) | 2 durumda |
| DMP1dentin matrix acidic phosphoprotein 1 | Çok sık (%80–99) | 2 durumda |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Çok sık (%80–99) | 1 durumda |
| LEMD3LEM domain containing 3 | Çok sık (%80–99) | 1 durumda |
| LRP4LDL receptor related protein 4 | Çok sık (%80–99) | 1 durumda |
| LRP5LDL receptor related protein 5 | Çok sık (%80–99) | 1 durumda |
| PTDSS1phosphatidylserine synthase 1 | Çok sık (%80–99) | 1 durumda |
| PTH1Rparathyroid hormone 1 receptor | Çok sık (%80–99) | 1 durumda |
| SLC26A2solute carrier family 26 member 2 | Çok sık (%80–99) | 1 durumda |
| SLC29A3solute carrier family 29 member 3 | Çok sık (%80–99) | 1 durumda |
| SOSTsclerostin | Çok sık (%80–99) | 2 durumda |
| TNFRSF11ATNF receptor superfamily member 11a | Çok sık (%80–99) | 1 durumda |
| DLX3distal-less homeobox 3 | Sık (%30–79) | 2 durumda |
| FLNAfilamin A | Sık (%30–79) | 2 durumda |
| GBA1glucosylceramidase beta 1 | Sık (%30–79) | 1 durumda |
| GNASGNAS complex locus | Sık (%30–79) | 3 durumda |
| LPIN2lipin 2 | Sık (%30–79) | 1 durumda |
| MITFmelanocyte inducing transcription factor | Sık (%30–79) | 1 durumda |
| TRAPPC2trafficking protein particle complex subunit 2 | Sık (%30–79) | 1 durumda |
| WRNWRN RecQ like helicase | Sık (%30–79) | 1 durumda |
| AARS1alanyl-tRNA synthetase 1 | Bazen (%5–29) | 1 durumda |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Bazen (%5–29) | 1 durumda |
| BMP1bone morphogenetic protein 1 | Bazen (%5–29) | 1 durumda |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Bazen (%5–29) | 1 durumda |
| CARS1cysteinyl-tRNA synthetase 1 | Bazen (%5–29) | 1 durumda |
| CLIP2CAP-Gly domain containing linker protein 2 | Bazen (%5–29) | 1 durumda |
| DBR1debranching RNA lariats 1 | Bazen (%5–29) | 1 durumda |
| DHCR2424-dehydrocholesterol reductase | Bazen (%5–29) | 2 durumda |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Bazen (%5–29) | 1 durumda |
| EIF4Heukaryotic translation initiation factor 4H | Bazen (%5–29) | 1 durumda |
| ELNelastin | Bazen (%5–29) | 1 durumda |
29 gen daha göster
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Bazen (%5–29) | 1 durumda |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Bazen (%5–29) | 1 durumda |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Bazen (%5–29) | 1 durumda |
| GTF2E2general transcription factor IIE subunit 2 | Bazen (%5–29) | 1 durumda |
| GTF2H5general transcription factor IIH subunit 5 | Bazen (%5–29) | 1 durumda |
| GTF2Igeneral transcription factor IIi | Bazen (%5–29) | 1 durumda |
| GTF2IRD1GTF2I repeat domain containing 1 | Bazen (%5–29) | 1 durumda |
| GTF2IRD2GTF2I repeat domain containing 2 | Bazen (%5–29) | 1 durumda |
| HSPG2heparan sulfate proteoglycan 2 | Bazen (%5–29) | 1 durumda |
| LIMK1LIM domain kinase 1 | Bazen (%5–29) | 1 durumda |
| LMNAlamin A/C | Bazen (%5–29) | 1 durumda |
| METTL27methyltransferase like 27 | Bazen (%5–29) | 1 durumda |
| MPLKIPM-phase specific PLK1 interacting protein | Bazen (%5–29) | 1 durumda |
| NCF1neutrophil cytosolic factor 1 | Bazen (%5–29) | 1 durumda |
| RFC2replication factor C subunit 2 | Bazen (%5–29) | 1 durumda |
| RNF113Aring finger protein 113A | Bazen (%5–29) | 1 durumda |
| STX16syntaxin 16 | Bazen (%5–29) | 1 durumda |
| STX1Asyntaxin 1A | Bazen (%5–29) | 1 durumda |
| TARS1threonyl-tRNA synthetase 1 | Bazen (%5–29) | 1 durumda |
| TBL2transducin beta like 2 | Bazen (%5–29) | 1 durumda |
| TMEM270transmembrane protein 270 | Bazen (%5–29) | 1 durumda |
| VPS37DVPS37D subunit of ESCRT-I | Bazen (%5–29) | 1 durumda |
| AGXTalanine--glyoxylate aminotransferase | Kaydedilmedi | 1 durumda |
| FAM111AFAM111 trypsin like peptidase A | Kaydedilmedi | 1 durumda |
| MAP2K1mitogen-activated protein kinase kinase 1 | Kaydedilmedi | 1 durumda |
| MC4Rmelanocortin 4 receptor | Kaydedilmedi | 1 durumda |
| RUNX2RUNX family transcription factor 2 | Kaydedilmedi | 1 durumda |
| TGFB1transforming growth factor beta 1 | Kaydedilmedi | 1 durumda |
| TNFRSF11BTNF receptor superfamily member 11b | 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
- Harder, denser, fracture-prone bones23 gen
- Dense bone of skull base16 gen
- Increased bone density in skeletal bones9 gen
- Cortical sclerosis5 gen
- Craniofacial osteosclerosis5 gen
- Increased calcification of skull4 gen
- Uneven increase in bone density3 gen
- Increased bone density in collarbone2 gen
- Increased bone density with cystic changes2 gen
- Increased density of long bones2 gen
- Osteopoikilosis2 gen
- Sclerotic scapulae2 gen
- Increased bone density in foot bone1 gen
- Increased bone density in hand bone1 gen
- Metacarpal diaphyseal endosteal sclerosis1 gen
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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