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Egenskap
Hip contracture
Lack of full passive range of motion (restrictions in flexion, extension, or other movements) of the hip joint resulting from structural changes of non-bony tissues, such as muscles, tendons, ligaments, joint capsules and/or skin.
Sammendrag
- Også kalt
- Flexion contracture of hips, Flexion contractures of hips, Hip contractures, Hip flexion contractures
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Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/hip-contracture.json"
page <- fromJSON(url)
page$trait$nameHip contractureHP:0003273
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Les genene knyttet til Hip contracture, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test44 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.
- Congenital MyopathiesReads 10 of these genesTNNT1ACTA1SELENONSPEGBIN1MAP3K20About this report →
- Immuno-Osseous DysplasiasReads 2 of these genesRMRPRNU4ATACAbout this report →
- Achondrogenesis panelReads 2 of these genesCOL2A1SLC26A2About this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
Show 40 more reports
- Congenital Muscular DystrophiesReads 4 of these genesCOL6A2COL6A3SELENONITGA7About this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Limb-Girdle Muscular DystrophyReads 4 of these genesCOL6A2COL6A3LMNATTNAbout this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1SLC26A2About this report →
- Marfan Like SyndromesReads 2 of these genesFBN2TGFB2About this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- HaemophiliaReads 1 of these genesF8About this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Spinal Muscular AtrophyReads 3 of these genesGARS1UBA1BICD2About this report →
- Myofibrillar MyopathiesReads 2 of these genesRYR1TTNAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGYPIGAAbout this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFB2About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 1 of these genesGNPATAbout this report →
- Congenital Myasthenic SyndromeReads 2 of these genesMUSKSCN4AAbout this report →
- Congenital Cranial Dysinnervation DisordersReads 1 of these genesCOL25A1About this report →
- Disorders of Glycine & Serine MetabolismReads 1 of these genesSLC6A9About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesGARS1LMNATRPV4About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesCOL6A3SCN4AAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Dilated CardiomyopathyReads 2 of these genesLMNATTNAbout this report →
- Aortic AneurysmReads 1 of these genesTGFB2About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesAPC2About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesMYL2NSD1About this report →
- Distal MyopathiesReads 1 of these genesTTNAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesPIGYPIGAAbout this report →
- VitreoretinopathyReads 1 of these genesCOL2A1About this report →
- Diabetes MellitusReads 1 of these genesZBTB20About this report →
- Osteogenesis ImperfectaReads 1 of these genesFKBP10About this report →
- DNA Repair DiseaseReads 1 of these genesERCC8About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGNPTABAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesERLIN2About this report →
- Leigh SyndromeReads 1 of these genesPNPT1About this report →
- Hearing Loss and DeafnessReads 1 of these genesPNPT1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesPNPT1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesPIGAAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesRMRPAbout this report →
- Intellectual DisabilityReads 1 of these genesZC4H2About this report →
Les genene knyttet til Hip contracture, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test64 gener knyttet til Hip contracture
Endringer i disse genene forårsaker sjeldne tilstander der Hip contracture forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| COL6A2collagen type VI alpha 2 chain | Alltid | I 1 tilstand |
| COL6A3collagen type VI alpha 3 chain | Alltid | I 1 tilstand |
| GARS1glycyl-tRNA synthetase 1 | Alltid | I 1 tilstand |
| GNB2G protein subunit beta 2 | Alltid | I 1 tilstand |
| GNPATglyceronephosphate O-acyltransferase | Alltid | I 1 tilstand |
| LGI4leucine rich repeat LGI family member 4 | Alltid | I 1 tilstand |
| NFATC2nuclear factor of activated T cells 2 | Alltid | I 1 tilstand |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Alltid | I 1 tilstand |
| TNNT1troponin T1, slow skeletal type | Alltid | I 3 tilstander |
| KAT6Blysine acetyltransferase 6B | Svært ofte (80–99 %) | I 2 tilstander |
| ZBTB20zinc finger and BTB domain containing 20 | Svært ofte (80–99 %) | I 2 tilstander |
| ACTA1actin alpha 1, skeletal muscle | Ofte (30–79 %) | I 2 tilstander |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Ofte (30–79 %) | I 1 tilstand |
| FILIP1filamin A interacting protein 1 | Ofte (30–79 %) | I 1 tilstand |
| HS2ST1heparan sulfate 2-O-sulfotransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| HSPG2heparan sulfate proteoglycan 2 | Ofte (30–79 %) | I 2 tilstander |
| LMNAlamin A/C | Ofte (30–79 %) | I 2 tilstander |
| MUSKmuscle associated receptor tyrosine kinase | Ofte (30–79 %) | I 1 tilstand |
| MYH3myosin heavy chain 3 | Ofte (30–79 %) | I 2 tilstander |
| MYL1myosin light chain 1 | Ofte (30–79 %) | I 1 tilstand |
| MYL11myosin light chain 11 | Ofte (30–79 %) | I 1 tilstand |
| NALCNsodium leak channel, non-selective | Ofte (30–79 %) | I 1 tilstand |
| PI4KAphosphatidylinositol 4-kinase alpha | Ofte (30–79 %) | I 1 tilstand |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Ofte (30–79 %) | I 1 tilstand |
| PPFIA3PPFI scaffold protein A3 | Ofte (30–79 %) | I 1 tilstand |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Ofte (30–79 %) | I 1 tilstand |
| RNU4ATACRNA, U4atac small nuclear | Ofte (30–79 %) | I 3 tilstander |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Ofte (30–79 %) | I 2 tilstander |
| SELENONselenoprotein N | Ofte (30–79 %) | I 2 tilstander |
| SPEGstriated muscle enriched protein kinase | Ofte (30–79 %) | I 2 tilstander |
| UBA1ubiquitin like modifier activating enzyme 1 | Ofte (30–79 %) | I 1 tilstand |
| BICD2BICD cargo adaptor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| BIN1bridging integrator 1 | Noen ganger (5–29 %) | I 1 tilstand |
| COL25A1collagen type XXV alpha 1 chain | Noen ganger (5–29 %) | I 1 tilstand |
| ERGIC1endoplasmic reticulum-golgi intermediate compartment 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ERLIN2ER lipid raft associated 2 | Noen ganger (5–29 %) | I 1 tilstand |
| FBN2fibrillin 2 | Noen ganger (5–29 %) | I 1 tilstand |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Noen ganger (5–29 %) | I 1 tilstand |
| HACD13-hydroxyacyl-CoA dehydratase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ITGA7integrin subunit alpha 7 | Noen ganger (5–29 %) | I 1 tilstand |
Vis 24 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Noen ganger (5–29 %) | I 1 tilstand |
| MYL2myosin light chain 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PNPT1polyribonucleotide nucleotidyltransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| RYR1ryanodine receptor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SCYL2SCY1 like pseudokinase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| TELO2telomere maintenance 2 | Noen ganger (5–29 %) | I 1 tilstand |
| TPM2tropomyosin 2 | Noen ganger (5–29 %) | I 2 tilstander |
| TPM3tropomyosin 3 | Noen ganger (5–29 %) | I 1 tilstand |
| TTNtitin | Noen ganger (5–29 %) | I 1 tilstand |
| UNC80unc-80 subunit of NALCN channel complex | Noen ganger (5–29 %) | I 1 tilstand |
| APC2APC regulator of Wnt signaling pathway 2 | Sjelden (1–4%) | I 1 tilstand |
| F8coagulation factor VIII | Sjelden (1–4%) | I 1 tilstand |
| NSD1nuclear receptor binding SET domain protein 1 | Sjelden (1–4%) | I 1 tilstand |
| COL2A1collagen type II alpha 1 chain | Ikke registrert | I 1 tilstand |
| FKBP10FKBP prolyl isomerase 10 | Ikke registrert | I 1 tilstand |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Ikke registrert | I 1 tilstand |
| MMP2matrix metallopeptidase 2 | Ikke registrert | I 1 tilstand |
| PTH1Rparathyroid hormone 1 receptor | Ikke registrert | I 1 tilstand |
| SLC10A7solute carrier family 10 member 7 | Ikke registrert | I 1 tilstand |
| SLC26A2solute carrier family 26 member 2 | Ikke registrert | I 1 tilstand |
| SLC6A9solute carrier family 6 member 9 | Ikke registrert | I 1 tilstand |
| TGFB2transforming growth factor beta 2 | Ikke registrert | I 1 tilstand |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Ikke registrert | I 1 tilstand |
| ZC4H2zinc finger C4H2-type containing | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Smalere egenskaper
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.18-8b139e39.
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