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Træk
Inability to straighten knee
Klinisk navn: Knee flexion contracture
A type of knee joint contracture in which the knee is in a fixed bent (flexed) configuration such that it cannot be straightened actively or passively.
Resumé
- Også kaldet
- Flexion contracture of knees, Flexion contractures at both knees, Flexion contractures of knees, Flexion deformity of the knee, Knee flexion contractures, Knee flexion deformity
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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/knee-flexion-contracture.json"
page <- fromJSON(url)
page$trait$nameInability to straighten kneeHP:0006380
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Læs de gener, der er knyttet til Inability to straighten knee, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test67 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 Myasthenic SyndromeReads 10 of these genesCHRNB1MYO9ASNAP25ALG2SLC18A3SYT2About this report →
- Congenital Muscular DystrophiesReads 7 of these genesCOL12A1COL6A1COL6A2COL6A3GMPPBITGA7About this report →
- Congenital MyopathiesReads 5 of these genesACTA1MAP3K20SELENONTPM2TPM3About this report →
- Congenital Disorders of GlycosylationReads 10 of these genesSRD5A3ALG2PIGAPIGYALG14COG8About this report →
Show 63 more reports
- CHRNG-Related Multiple Pterygium SyndromeReads 1 of these genesCHRNGAbout this report →
- Dystrophinopathies (Duchenne and Becker Muscular Dystrophy)Reads 1 of these genesDMDAbout this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- KAT6B-Related DisordersReads 1 of these genesKAT6BAbout this report →
- Nail-Patella SyndromeReads 1 of these genesLMX1BAbout this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- Primrose SyndromeReads 1 of these genesZBTB20About this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Roberts SyndromeReads 1 of these genesESCO2About this report →
- RTTN-Related Microcephalic Primordial DwarfismReads 1 of these genesRTTNAbout this report →
- Spondylo-Meta-Epiphyseal Dysplasia, Short Limb-Abnormal Calcification TypeReads 1 of these genesDDR2About this report →
- Stüve-Wiedemann SyndromeReads 1 of these genesLIFRAbout this report →
- TRPV4-Related Skeletal DysplasiasReads 1 of these genesTRPV4About this report →
- You-Hoover-Fong Syndrome (TELO2)Reads 1 of these genesTELO2About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 3 of these genesSDHASDHBSDHDAbout this report →
- Marfan Like SyndromesReads 3 of these genesFBN2FBN1TGFB2About this report →
- Periventricular Nodular HeterotopiaReads 2 of these genesNEDD4LFLNAAbout this report →
- Limb-Girdle Muscular DystrophyReads 5 of these genesCOL6A1COL6A2COL6A3GMPPBJAG2About this report →
- Myofibrillar MyopathiesReads 3 of these genesSVILKYBAG3About this report →
- Malignant Endocrine NeoplasmReads 2 of these genesSDHASDHBAbout this report →
- Urinary and Renal System TumourReads 2 of these genesSDHASDHBAbout this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRNU4ATACAbout this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Dilated CardiomyopathyReads 4 of these genesDMDEMDFHL1BAG3About this report →
- Aortic AneurysmReads 2 of these genesFBN1TGFB2About this report →
- Hereditary Gastrointestinal Stromal TumourReads 1 of these genesSDHBAbout this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGAPIGYAbout this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3R2About this report →
- Inherited Neurodegenerative DisordersReads 8 of these genesERLIN2NT5C2NALCNUBA1BICD2ERLIN1About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFB2About this report →
- Spinal Muscular AtrophyReads 2 of these genesUBA1BICD2About this report →
- Congenital Cranial Dysinnervation DisordersReads 1 of these genesCOL25A1About this report →
- Hereditary Spastic ParaplegiaReads 3 of these genesERLIN2NT5C2ERLIN1About this report →
- Disorders of Glycine & Serine MetabolismReads 1 of these genesPSAT1About this report →
- Osteogenesis ImperfectaReads 2 of these genesFKBP10PLOD2About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 2 of these genesGJB2GJB6About this report →
- Kidney CancerReads 1 of these genesSDHBAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 5 of these genesBICD2SDHASLC25A46TRIM2TRPV4About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesC19orf12About this report →
- DNA Repair DiseaseReads 2 of these genesERCC1ERCC6About this report →
- Epilepsy (Full Panel)Reads 4 of these genesSNAP25PIGASLC6A1FLNAAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Cutis LaxaReads 1 of these genesATP6V1E1About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesCPT2About this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesANKLE2About this report →
- Ectodermal DysplasiasReads 1 of these genesGJB6About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesTRIM2TRPV4About this report →
- Autoimmune DiseaseReads 1 of these genesCHRNGAbout this report →
- Ehlers-Danlos SyndromeReads 1 of these genesCOL12A1About this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesSLC25A46About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesPSAT1About this report →
- Syndromic CraniosynostosisReads 1 of these genesMEGF8About this report →
- Hearing Loss and DeafnessReads 2 of these genesGJB2GJB6About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesGLI3About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesERCC1About this report →
- Diabetes MellitusReads 1 of these genesZBTB20About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesPSTPIP1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesCOL6A3About this report →
- Intellectual DisabilityReads 2 of these genesTAF4RPL10About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGNPTABAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesMYL2About this report →
- Leigh SyndromeReads 1 of these genesSDHAAbout this report →
Læs de gener, der er knyttet til Inability to straighten knee, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test109 gener knyttet til Inability to straighten knee
Ændringer i disse gener forårsager sjældne tilstande, hvor Inability to straighten knee 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 |
|---|---|---|
| CHRNB1cholinergic receptor nicotinic beta 1 subunit | Altid | I 1 tilstand |
| CHRNGcholinergic receptor nicotinic gamma subunit | Altid | I 1 tilstand |
| DMDdystrophin | Altid | I 1 tilstand |
| DONSONDNA replication fork stabilization factor DONSON | Altid | I 1 tilstand |
| EMDemerin | Altid | I 1 tilstand |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Altid | I 1 tilstand |
| FBN2fibrillin 2 | Altid | I 1 tilstand |
| FKBP10FKBP prolyl isomerase 10 | Altid | I 1 tilstand |
| GNB2G protein subunit beta 2 | Altid | I 1 tilstand |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Altid | I 2 tilstande |
| KLC4kinesin light chain 4 | Altid | I 1 tilstand |
| LBRlamin B receptor | Altid | I 1 tilstand |
| LGI4leucine rich repeat LGI family member 4 | Altid | I 1 tilstand |
| MAU2MAU2 sister chromatid cohesion factor | Altid | I 1 tilstand |
| MYO9Amyosin IXA | Altid | I 1 tilstand |
| NFATC2nuclear factor of activated T cells 2 | Altid | I 1 tilstand |
| PSTPIP1proline-serine-threonine phosphatase interacting protein 1 | Altid | I 1 tilstand |
| SIK3SIK family kinase 3 | Altid | I 1 tilstand |
| SNAP25synaptosome associated protein 25 | Altid | I 1 tilstand |
| SRD5A3steroid 5 alpha-reductase 3 | Altid | I 1 tilstand |
| TAF4TATA-box binding protein associated factor 4 | Altid | I 1 tilstand |
| ADAMTS15ADAM metallopeptidase with thrombospondin type 1 motif 15 | Meget ofte (80–99 %) | I 1 tilstand |
| ERLIN2ER lipid raft associated 2 | Meget ofte (80–99 %) | I 2 tilstande |
| FBN1fibrillin 1 | Meget ofte (80–99 %) | I 1 tilstand |
| KAT6Blysine acetyltransferase 6B | Meget ofte (80–99 %) | I 2 tilstande |
| NT5C25'-nucleotidase, cytosolic II | Meget ofte (80–99 %) | I 1 tilstand |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Ofte (30–79 %) | I 2 tilstande |
| ANKLE2ankyrin repeat and LEM domain containing 2 | Ofte (30–79 %) | I 1 tilstand |
| COL12A1collagen type XII alpha 1 chain | Ofte (30–79 %) | I 2 tilstande |
| COL25A1collagen type XXV alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| COL6A1collagen type VI alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| COL6A2collagen type VI alpha 2 chain | Ofte (30–79 %) | I 1 tilstand |
| COL6A3collagen type VI alpha 3 chain | Ofte (30–79 %) | I 1 tilstand |
| ERGIC1endoplasmic reticulum-golgi intermediate compartment 1 | Ofte (30–79 %) | I 1 tilstand |
| FDFT1farnesyl-diphosphate farnesyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| GLI3GLI family zinc finger 3 | Ofte (30–79 %) | I 1 tilstand |
| HS2ST1heparan sulfate 2-O-sulfotransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| LIFRLIF receptor subunit alpha | Ofte (30–79 %) | I 2 tilstande |
| MYH3myosin heavy chain 3 | Ofte (30–79 %) | I 2 tilstande |
| MYL1myosin light chain 1 | Ofte (30–79 %) | I 1 tilstand |
Vis 69 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| 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 3 tilstande |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Ofte (30–79 %) | I 1 tilstand |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Ofte (30–79 %) | I 1 tilstand |
| RPL10ribosomal protein L10 | Ofte (30–79 %) | I 1 tilstand |
| SCYL2SCY1 like pseudokinase 2 | Ofte (30–79 %) | I 1 tilstand |
| SLC18A3solute carrier family 18 member A3 | Ofte (30–79 %) | I 1 tilstand |
| SVILsupervillin | Ofte (30–79 %) | I 1 tilstand |
| SYT2synaptotagmin 2 | Ofte (30–79 %) | I 1 tilstand |
| UBA1ubiquitin like modifier activating enzyme 1 | Ofte (30–79 %) | I 1 tilstand |
| ACTA1actin alpha 1, skeletal muscle | Nogle gange (5–29 %) | I 1 tilstand |
| ALG14ALG14 UDP-N-acetylglucosaminyltransferase subunit | Nogle gange (5–29 %) | I 1 tilstand |
| BICD2BICD cargo adaptor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| COG8component of oligomeric golgi complex 8 | Nogle gange (5–29 %) | I 1 tilstand |
| DHX16DEAH-box helicase 16 | Nogle gange (5–29 %) | I 1 tilstand |
| DPAGT1dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| DPM1dolichyl-phosphate mannosyltransferase subunit 1, catalytic | Nogle gange (5–29 %) | I 2 tilstande |
| ERLIN1ER lipid raft associated 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Nogle gange (5–29 %) | I 2 tilstande |
| FHL1four and a half LIM domains 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GFPT1glutamine--fructose-6-phosphate transaminase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GMPPBGDP-mannose pyrophosphorylase B | Nogle gange (5–29 %) | I 1 tilstand |
| HACD13-hydroxyacyl-CoA dehydratase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ITGA7integrin subunit alpha 7 | Nogle gange (5–29 %) | I 1 tilstand |
| JAG2jagged canonical Notch ligand 2 | Nogle gange (5–29 %) | I 1 tilstand |
| KYkyphoscoliosis peptidase | Nogle gange (5–29 %) | I 1 tilstand |
| LMBRD2LMBR1 domain containing 2 | Nogle gange (5–29 %) | I 1 tilstand |
| LMX1BLIM homeobox transcription factor 1 beta | Nogle gange (5–29 %) | I 1 tilstand |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Nogle gange (5–29 %) | I 1 tilstand |
| MEGF8multiple EGF like domains 8 | Nogle gange (5–29 %) | I 1 tilstand |
| MYL2myosin light chain 2 | Nogle gange (5–29 %) | I 1 tilstand |
| NEDD4LNEDD4 like E3 ubiquitin protein ligase | Nogle gange (5–29 %) | I 1 tilstand |
| PSAT1phosphoserine aminotransferase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RTTNrotatin | Nogle gange (5–29 %) | I 1 tilstand |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Nogle gange (5–29 %) | I 1 tilstand |
| SDHAF1succinate dehydrogenase complex assembly factor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Nogle gange (5–29 %) | I 1 tilstand |
| SDHDsuccinate dehydrogenase complex subunit D | Nogle gange (5–29 %) | I 1 tilstand |
| SELENONselenoprotein N | Nogle gange (5–29 %) | I 1 tilstand |
| SLC25A46solute carrier family 25 member 46 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC39A8solute carrier family 39 member 8 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC6A1solute carrier family 6 member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC6A11solute carrier family 6 member 11 | Nogle gange (5–29 %) | I 1 tilstand |
| TELO2telomere maintenance 2 | Nogle gange (5–29 %) | I 1 tilstand |
| TPM2tropomyosin 2 | Nogle gange (5–29 %) | I 2 tilstande |
| TPM3tropomyosin 3 | Nogle gange (5–29 %) | I 1 tilstand |
| UFC1ubiquitin-fold modifier conjugating enzyme 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GJB2gap junction protein beta 2 | Sjældent (1–4%) | I 2 tilstande |
| GJB6gap junction protein beta 6 | Sjældent (1–4%) | I 1 tilstand |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Ikke registreret | I 1 tilstand |
| BAG3BAG cochaperone 3 | Ikke registreret | I 1 tilstand |
| C19orf12chromosome 19 open reading frame 12 | Ikke registreret | I 1 tilstand |
| CNTNAP1contactin associated protein 1 | Ikke registreret | I 1 tilstand |
| CPT2carnitine palmitoyltransferase 2 | Ikke registreret | I 1 tilstand |
| DDR2discoidin domain receptor tyrosine kinase 2 | Ikke registreret | I 1 tilstand |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Ikke registreret | I 1 tilstand |
| FLNAfilamin A | Ikke registreret | I 1 tilstand |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Ikke registreret | I 1 tilstand |
| PIK3R2phosphoinositide-3-kinase regulatory subunit 2 | Ikke registreret | I 1 tilstand |
| PLOD2procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 | Ikke registreret | I 1 tilstand |
| PTDSS1phosphatidylserine synthase 1 | Ikke registreret | I 1 tilstand |
| PTH1Rparathyroid hormone 1 receptor | Ikke registreret | I 1 tilstand |
| RNU4ATACRNA, U4atac small nuclear | Ikke registreret | I 1 tilstand |
| SCARF2scavenger receptor class F member 2 | Ikke registreret | I 1 tilstand |
| TGFB2transforming growth factor beta 2 | Ikke registreret | I 1 tilstand |
| TRIM2tripartite motif containing 2 | Ikke registreret | I 1 tilstand |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Ikke registreret | I 1 tilstand |
| ZBTB20zinc finger and BTB domain containing 20 | 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.
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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