Tratto
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.
Riepilogo
- Detto anche
- Increased bone density, Osteosclerosis, Osteosclerosis of bones
- Sistema corporeo
- Abnormality of the musculoskeletal system
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Ottieni il mio Genome Test60 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 →
Leggi i geni collegati a Increased bone mineral density e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test69 geni collegati a Increased bone mineral density
Alterazioni in questi geni causano malattie rare in cui si osserva Increased bone mineral density. La maggior parte delle persone con questo tratto non presenta nessuna di tali condizioni, e un gene di questo elenco non dice nulla sul genoma di nessuno in particolare.
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| AXIN1axin 1 | Sempre | In 1 condizione |
| CLCN7Cl-/H+ antiporter 7 | Sempre | In 1 condizione |
| FAM20CFAM20C golgi associated secretory pathway kinase | Sempre | In 1 condizione |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Sempre | In 1 condizione |
| SLC4A2solute carrier family 4 member 2 | Sempre | In 1 condizione |
| TBXAS1thromboxane A synthase 1 | Sempre | In 1 condizione |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Sempre | In 2 condizioni |
| AMER1APC membrane recruitment protein 1 | Molto spesso (80–99%) | In 1 condizione |
| CTNNB1catenin beta 1 | Molto spesso (80–99%) | In 1 condizione |
| CTSKcathepsin K | Molto spesso (80–99%) | In 2 condizioni |
| DMP1dentin matrix acidic phosphoprotein 1 | Molto spesso (80–99%) | In 2 condizioni |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Molto spesso (80–99%) | In 1 condizione |
| LEMD3LEM domain containing 3 | Molto spesso (80–99%) | In 1 condizione |
| LRP4LDL receptor related protein 4 | Molto spesso (80–99%) | In 1 condizione |
| LRP5LDL receptor related protein 5 | Molto spesso (80–99%) | In 1 condizione |
| PTDSS1phosphatidylserine synthase 1 | Molto spesso (80–99%) | In 1 condizione |
| PTH1Rparathyroid hormone 1 receptor | Molto spesso (80–99%) | In 1 condizione |
| SLC26A2solute carrier family 26 member 2 | Molto spesso (80–99%) | In 1 condizione |
| SLC29A3solute carrier family 29 member 3 | Molto spesso (80–99%) | In 1 condizione |
| SOSTsclerostin | Molto spesso (80–99%) | In 2 condizioni |
| TNFRSF11ATNF receptor superfamily member 11a | Molto spesso (80–99%) | In 1 condizione |
| DLX3distal-less homeobox 3 | Spesso (30–79%) | In 2 condizioni |
| FLNAfilamin A | Spesso (30–79%) | In 2 condizioni |
| GBA1glucosylceramidase beta 1 | Spesso (30–79%) | In 1 condizione |
| GNASGNAS complex locus | Spesso (30–79%) | In 3 condizioni |
| LPIN2lipin 2 | Spesso (30–79%) | In 1 condizione |
| MITFmelanocyte inducing transcription factor | Spesso (30–79%) | In 1 condizione |
| TRAPPC2trafficking protein particle complex subunit 2 | Spesso (30–79%) | In 1 condizione |
| WRNWRN RecQ like helicase | Spesso (30–79%) | In 1 condizione |
| AARS1alanyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | A volte (5–29%) | In 1 condizione |
| BMP1bone morphogenetic protein 1 | A volte (5–29%) | In 1 condizione |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | A volte (5–29%) | In 1 condizione |
| CARS1cysteinyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| CLIP2CAP-Gly domain containing linker protein 2 | A volte (5–29%) | In 1 condizione |
| DBR1debranching RNA lariats 1 | A volte (5–29%) | In 1 condizione |
| DHCR2424-dehydrocholesterol reductase | A volte (5–29%) | In 2 condizioni |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | A volte (5–29%) | In 1 condizione |
| EIF4Heukaryotic translation initiation factor 4H | A volte (5–29%) | In 1 condizione |
| ELNelastin | A volte (5–29%) | In 1 condizione |
Mostra altri 29 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | A volte (5–29%) | In 1 condizione |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | A volte (5–29%) | In 1 condizione |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | A volte (5–29%) | In 1 condizione |
| GTF2E2general transcription factor IIE subunit 2 | A volte (5–29%) | In 1 condizione |
| GTF2H5general transcription factor IIH subunit 5 | A volte (5–29%) | In 1 condizione |
| GTF2Igeneral transcription factor IIi | A volte (5–29%) | In 1 condizione |
| GTF2IRD1GTF2I repeat domain containing 1 | A volte (5–29%) | In 1 condizione |
| GTF2IRD2GTF2I repeat domain containing 2 | A volte (5–29%) | In 1 condizione |
| HSPG2heparan sulfate proteoglycan 2 | A volte (5–29%) | In 1 condizione |
| LIMK1LIM domain kinase 1 | A volte (5–29%) | In 1 condizione |
| LMNAlamin A/C | A volte (5–29%) | In 1 condizione |
| METTL27methyltransferase like 27 | A volte (5–29%) | In 1 condizione |
| MPLKIPM-phase specific PLK1 interacting protein | A volte (5–29%) | In 1 condizione |
| NCF1neutrophil cytosolic factor 1 | A volte (5–29%) | In 1 condizione |
| RFC2replication factor C subunit 2 | A volte (5–29%) | In 1 condizione |
| RNF113Aring finger protein 113A | A volte (5–29%) | In 1 condizione |
| STX16syntaxin 16 | A volte (5–29%) | In 1 condizione |
| STX1Asyntaxin 1A | A volte (5–29%) | In 1 condizione |
| TARS1threonyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| TBL2transducin beta like 2 | A volte (5–29%) | In 1 condizione |
| TMEM270transmembrane protein 270 | A volte (5–29%) | In 1 condizione |
| VPS37DVPS37D subunit of ESCRT-I | A volte (5–29%) | In 1 condizione |
| AGXTalanine--glyoxylate aminotransferase | Non registrato | In 1 condizione |
| FAM111AFAM111 trypsin like peptidase A | Non registrato | In 1 condizione |
| MAP2K1mitogen-activated protein kinase kinase 1 | Non registrato | In 1 condizione |
| MC4Rmelanocortin 4 receptor | Non registrato | In 1 condizione |
| RUNX2RUNX family transcription factor 2 | Non registrato | In 1 condizione |
| TGFB1transforming growth factor beta 1 | Non registrato | In 1 condizione |
| TNFRSF11BTNF receptor superfamily member 11b | Non registrato | In 1 condizione |
Con quale frequenza questo tratto si presenta tra le persone con una delle condizioni legate al gene, nella misura più alta riscontrata tra queste, secondo quanto registrato dall'Human Phenotype Ontology. Queste pagine descrivono tratti e la ricerca che li riguarda; non costituiscono una diagnosi, e per i sintomi il medico o il consulente genetico è la persona a cui rivolgersi.
Tratti più specifici
- Harder, denser, fracture-prone bones23 geni
- Dense bone of skull base16 geni
- Increased bone density in skeletal bones9 geni
- Cortical sclerosis5 geni
- Craniofacial osteosclerosis5 geni
- Increased calcification of skull4 geni
- Uneven increase in bone density3 geni
- Increased bone density in collarbone2 geni
- Increased bone density with cystic changes2 geni
- Increased density of long bones2 geni
- Osteopoikilosis2 geni
- Sclerotic scapulae2 geni
- Increased bone density in foot bone1 gene
- Increased bone density in hand bone1 gene
- Metacarpal diaphyseal endosteal sclerosis1 gene
Tratti più generali
Fonte dei dati
- Human Phenotype Ontology, versione 2026-09-01: il tratto, i suoi nomi, la sua definizione e i geni a esso collegati. Per saperne di più visiti hpo.jax.org.
- Versione dei dati 2026.10.19-9814e911.
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