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Træk
Abnormal cortical bone morphology
An abnormality of compact bone (also known as cortical bone), which forms the dense surface of bones.
Resumé
- Også kaldet
- Abnormal compact bone morphology, Abnormality of cortical bone
- Kropssystem
- Abnormality of the musculoskeletal system
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Denne 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/abnormal-cortical-bone-morphology.json"
page <- fromJSON(url)
page$trait$nameAbnormal cortical bone morphologyHP:0003103
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Læs de gener, der er knyttet til Abnormal cortical bone morphology, og resten af dit genom, med én test.
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Bestil min Genome Test33 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.
- Autosomal Recessive Primary MicrocephalyReads 15 of these genesANKLE2ASPMCDK5RAP2CEP135CEP152CITAbout this report →
- Cenani-Lenz Syndactyly SyndromeReads 1 of these genesLRP4About this report →
- Ghosal Haematodiaphyseal DysplasiaReads 1 of these genesTBXAS1About this report →
- MCPH1-Related Primary MicrocephalyReads 1 of these genesMCPH1About this report →
Show 29 more reports
- Stüve-Wiedemann SyndromeReads 1 of these genesLIFRAbout this report →
- TRPV4-Related Skeletal DysplasiasReads 1 of these genesTRPV4About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 2 of these genesLRP5SOSTAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 4 of these genesKIF1ARETREG1SCN9AWNK1About this report →
- Monogenic Early-Onset OsteoporosisReads 1 of these genesCOPB2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 8 of these genesKIF1ARETREG1SCN9ATRPV4WNK1SARS1About this report →
- Polycystic Liver Disease (1 and 2)Reads 1 of these genesLRP5About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesAGAAbout this report →
- Meckel SyndromeReads 1 of these genesKIF14About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- OsteopetrosisReads 1 of these genesLRP5About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX19About this report →
- Intellectual DisabilityReads 4 of these genesKIF1AMETTL5TAF13NSDHLAbout this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesWNK1About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesTRPV4WARS1About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesPYCR2PEX19About this report →
- Inherited Neurodegenerative DisordersReads 4 of these genesKIF1APYCR2WARS1PEX19About this report →
- Inherited IchthyosesReads 1 of these genesNSDHLAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPYCR2About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesLRP4About this report →
- VitreoretinopathyReads 1 of these genesLRP5About this report →
- Spinal Muscular AtrophyReads 1 of these genesWARS1About this report →
- Osteogenesis ImperfectaReads 1 of these genesLRP5About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesGJA1About this report →
- Epilepsy (Full Panel)Reads 2 of these genesFLNASCN9AAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesAGAAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesKIF1AAbout this report →
Læs de gener, der er knyttet til Abnormal cortical bone morphology, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test49 gener knyttet til Abnormal cortical bone morphology
Ændringer i disse gener forårsager sjældne tilstande, hvor Abnormal cortical bone morphology 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 |
|---|---|---|
| FLNAfilamin A | Meget ofte (80–99 %) | I 1 tilstand |
| HPGD15-hydroxyprostaglandin dehydrogenase | Meget ofte (80–99 %) | I 2 tilstande |
| KIF1Akinesin family member 1A | Meget ofte (80–99 %) | I 1 tilstand |
| LEMD3LEM domain containing 3 | Meget ofte (80–99 %) | I 1 tilstand |
| LIFRLIF receptor subunit alpha | Meget ofte (80–99 %) | I 1 tilstand |
| LRP4LDL receptor related protein 4 | Meget ofte (80–99 %) | I 1 tilstand |
| LRP5LDL receptor related protein 5 | Meget ofte (80–99 %) | I 2 tilstande |
| PTDSS1phosphatidylserine synthase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| RETREG1reticulophagy regulator 1 | Meget ofte (80–99 %) | I 1 tilstand |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Meget ofte (80–99 %) | I 1 tilstand |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Meget ofte (80–99 %) | I 1 tilstand |
| SOSTsclerostin | Meget ofte (80–99 %) | I 2 tilstande |
| TBXAS1thromboxane A synthase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Meget ofte (80–99 %) | I 1 tilstand |
| WNK1WNK lysine deficient protein kinase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| AGAaspartylglucosaminidase | Ofte (30–79 %) | I 1 tilstand |
| ANKLE2ankyrin repeat and LEM domain containing 2 | Ofte (30–79 %) | I 1 tilstand |
| ASPMassembly factor for spindle microtubules | Ofte (30–79 %) | I 1 tilstand |
| CDK5RAP2CDK5 regulatory subunit associated protein 2 | Ofte (30–79 %) | I 1 tilstand |
| CDK6cyclin dependent kinase 6 | Ofte (30–79 %) | I 1 tilstand |
| CENPEcentromere protein E | Ofte (30–79 %) | I 1 tilstand |
| CEP135centrosomal protein 135 | Ofte (30–79 %) | I 1 tilstand |
| CEP152centrosomal protein 152 | Ofte (30–79 %) | I 1 tilstand |
| CITcitron rho-interacting serine/threonine kinase | Ofte (30–79 %) | I 1 tilstand |
| COPB2coat protein complex I subunit beta 2 | Ofte (30–79 %) | I 1 tilstand |
| CPAPcentrosome assembly and centriole elongation protein | Ofte (30–79 %) | I 1 tilstand |
| GJA1gap junction protein alpha 1 | Ofte (30–79 %) | I 1 tilstand |
| GLE1GLE1 RNA export mediator | Ofte (30–79 %) | I 1 tilstand |
| KIF14kinesin family member 14 | Ofte (30–79 %) | I 1 tilstand |
| KNL1kinetochore scaffold 1 | Ofte (30–79 %) | I 1 tilstand |
| MCM7minichromosome maintenance complex component 7 | Ofte (30–79 %) | I 1 tilstand |
| MCPH1microcephalin 1 | Ofte (30–79 %) | I 1 tilstand |
| METTL5methyltransferase 5, N6-adenosine | Ofte (30–79 %) | I 1 tilstand |
| MFSD2AMFSD2 lysolipid transporter A, lysophospholipid | Ofte (30–79 %) | I 1 tilstand |
| NCAPD3non-SMC condensin II complex subunit D3 | Ofte (30–79 %) | I 1 tilstand |
| NUP37nucleoporin 37 | Ofte (30–79 %) | I 1 tilstand |
| PDCD6IPprogrammed cell death 6 interacting protein | Ofte (30–79 %) | I 1 tilstand |
| PHC1polyhomeotic homolog 1 | Ofte (30–79 %) | I 1 tilstand |
| PYCR2pyrroline-5-carboxylate reductase 2 | Ofte (30–79 %) | I 1 tilstand |
| SARS1seryl-tRNA synthetase 1 | Ofte (30–79 %) | I 1 tilstand |
Vis 9 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| SASS6SAS-6 centriolar assembly protein | Ofte (30–79 %) | I 1 tilstand |
| STILSTIL centriolar assembly protein | Ofte (30–79 %) | I 1 tilstand |
| TAF13TATA-box binding protein associated factor 13 | Ofte (30–79 %) | I 1 tilstand |
| TRAPPC10trafficking protein particle complex subunit 10 | Ofte (30–79 %) | I 1 tilstand |
| TRAPPC14trafficking protein particle complex subunit 14 | Ofte (30–79 %) | I 1 tilstand |
| WARS1tryptophanyl-tRNA synthetase 1 | Ofte (30–79 %) | I 1 tilstand |
| WDR62WD repeat domain 62 | Ofte (30–79 %) | I 1 tilstand |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Ikke registreret | I 1 tilstand |
| PEX19peroxisomal biogenesis factor 19 | 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.
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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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