AtlasHvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørSekvenser genomet ditt↗
Egenskap
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.
Sammendrag
- Også kalt
- Flexion contracture of knees, Flexion contractures at both knees, Flexion contractures of knees, Flexion deformity of the knee, Knee flexion contractures, Knee flexion deformity
AtlasHvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørSekvenser genomet ditt↗
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/knee-flexion-contracture.json"
page <- fromJSON(url)
page$trait$nameInability to straighten kneeHP:0006380
AtlasHvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørSekvenser genomet ditt↗
Les genene knyttet til Inability to straighten knee, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt 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 →
Les genene knyttet til Inability to straighten knee, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test109 gener knyttet til Inability to straighten knee
Endringer i disse genene forårsaker sjeldne tilstander der Inability to straighten knee 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 |
|---|---|---|
| CHRNB1cholinergic receptor nicotinic beta 1 subunit | Alltid | I 1 tilstand |
| CHRNGcholinergic receptor nicotinic gamma subunit | Alltid | I 1 tilstand |
| DMDdystrophin | Alltid | I 1 tilstand |
| DONSONDNA replication fork stabilization factor DONSON | Alltid | I 1 tilstand |
| EMDemerin | Alltid | I 1 tilstand |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Alltid | I 1 tilstand |
| FBN2fibrillin 2 | Alltid | I 1 tilstand |
| FKBP10FKBP prolyl isomerase 10 | Alltid | I 1 tilstand |
| GNB2G protein subunit beta 2 | Alltid | I 1 tilstand |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Alltid | I 2 tilstander |
| KLC4kinesin light chain 4 | Alltid | I 1 tilstand |
| LBRlamin B receptor | Alltid | I 1 tilstand |
| LGI4leucine rich repeat LGI family member 4 | Alltid | I 1 tilstand |
| MAU2MAU2 sister chromatid cohesion factor | Alltid | I 1 tilstand |
| MYO9Amyosin IXA | Alltid | I 1 tilstand |
| NFATC2nuclear factor of activated T cells 2 | Alltid | I 1 tilstand |
| PSTPIP1proline-serine-threonine phosphatase interacting protein 1 | Alltid | I 1 tilstand |
| SIK3SIK family kinase 3 | Alltid | I 1 tilstand |
| SNAP25synaptosome associated protein 25 | Alltid | I 1 tilstand |
| SRD5A3steroid 5 alpha-reductase 3 | Alltid | I 1 tilstand |
| TAF4TATA-box binding protein associated factor 4 | Alltid | I 1 tilstand |
| ADAMTS15ADAM metallopeptidase with thrombospondin type 1 motif 15 | Svært ofte (80–99 %) | I 1 tilstand |
| ERLIN2ER lipid raft associated 2 | Svært ofte (80–99 %) | I 2 tilstander |
| FBN1fibrillin 1 | Svært ofte (80–99 %) | I 1 tilstand |
| KAT6Blysine acetyltransferase 6B | Svært ofte (80–99 %) | I 2 tilstander |
| NT5C25'-nucleotidase, cytosolic II | Svært ofte (80–99 %) | I 1 tilstand |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Ofte (30–79 %) | I 2 tilstander |
| ANKLE2ankyrin repeat and LEM domain containing 2 | Ofte (30–79 %) | I 1 tilstand |
| COL12A1collagen type XII alpha 1 chain | Ofte (30–79 %) | I 2 tilstander |
| 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 tilstander |
| MYH3myosin heavy chain 3 | Ofte (30–79 %) | I 2 tilstander |
| MYL1myosin light chain 1 | Ofte (30–79 %) | I 1 tilstand |
Vis 69 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| 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 tilstander |
| 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 | Noen ganger (5–29 %) | I 1 tilstand |
| ALG14ALG14 UDP-N-acetylglucosaminyltransferase subunit | Noen ganger (5–29 %) | I 1 tilstand |
| BICD2BICD cargo adaptor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| COG8component of oligomeric golgi complex 8 | Noen ganger (5–29 %) | I 1 tilstand |
| DHX16DEAH-box helicase 16 | Noen ganger (5–29 %) | I 1 tilstand |
| DPAGT1dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DPM1dolichyl-phosphate mannosyltransferase subunit 1, catalytic | Noen ganger (5–29 %) | I 2 tilstander |
| ERLIN1ER lipid raft associated 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Noen ganger (5–29 %) | I 2 tilstander |
| FHL1four and a half LIM domains 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GFPT1glutamine--fructose-6-phosphate transaminase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GMPPBGDP-mannose pyrophosphorylase B | 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 |
| JAG2jagged canonical Notch ligand 2 | Noen ganger (5–29 %) | I 1 tilstand |
| KYkyphoscoliosis peptidase | Noen ganger (5–29 %) | I 1 tilstand |
| LMBRD2LMBR1 domain containing 2 | Noen ganger (5–29 %) | I 1 tilstand |
| LMX1BLIM homeobox transcription factor 1 beta | Noen ganger (5–29 %) | I 1 tilstand |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Noen ganger (5–29 %) | I 1 tilstand |
| MEGF8multiple EGF like domains 8 | Noen ganger (5–29 %) | I 1 tilstand |
| MYL2myosin light chain 2 | Noen ganger (5–29 %) | I 1 tilstand |
| NEDD4LNEDD4 like E3 ubiquitin protein ligase | Noen ganger (5–29 %) | I 1 tilstand |
| PSAT1phosphoserine aminotransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| RTTNrotatin | Noen ganger (5–29 %) | I 1 tilstand |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Noen ganger (5–29 %) | I 1 tilstand |
| SDHAF1succinate dehydrogenase complex assembly factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Noen ganger (5–29 %) | I 1 tilstand |
| SDHDsuccinate dehydrogenase complex subunit D | Noen ganger (5–29 %) | I 1 tilstand |
| SELENONselenoprotein N | Noen ganger (5–29 %) | I 1 tilstand |
| SLC25A46solute carrier family 25 member 46 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC39A8solute carrier family 39 member 8 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC6A1solute carrier family 6 member 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC6A11solute carrier family 6 member 11 | 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 |
| UFC1ubiquitin-fold modifier conjugating enzyme 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GJB2gap junction protein beta 2 | Sjelden (1–4%) | I 2 tilstander |
| GJB6gap junction protein beta 6 | Sjelden (1–4%) | I 1 tilstand |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Ikke registrert | I 1 tilstand |
| BAG3BAG cochaperone 3 | Ikke registrert | I 1 tilstand |
| C19orf12chromosome 19 open reading frame 12 | Ikke registrert | I 1 tilstand |
| CNTNAP1contactin associated protein 1 | Ikke registrert | I 1 tilstand |
| CPT2carnitine palmitoyltransferase 2 | Ikke registrert | I 1 tilstand |
| DDR2discoidin domain receptor tyrosine kinase 2 | Ikke registrert | I 1 tilstand |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Ikke registrert | I 1 tilstand |
| FLNAfilamin A | Ikke registrert | I 1 tilstand |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Ikke registrert | I 1 tilstand |
| PIK3R2phosphoinositide-3-kinase regulatory subunit 2 | Ikke registrert | I 1 tilstand |
| PLOD2procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 | Ikke registrert | I 1 tilstand |
| PTDSS1phosphatidylserine synthase 1 | Ikke registrert | I 1 tilstand |
| PTH1Rparathyroid hormone 1 receptor | Ikke registrert | I 1 tilstand |
| RNU4ATACRNA, U4atac small nuclear | Ikke registrert | I 1 tilstand |
| SCARF2scavenger receptor class F member 2 | Ikke registrert | I 1 tilstand |
| TGFB2transforming growth factor beta 2 | Ikke registrert | I 1 tilstand |
| TRIM2tripartite motif containing 2 | Ikke registrert | I 1 tilstand |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Ikke registrert | I 1 tilstand |
| ZBTB20zinc finger and BTB domain containing 20 | 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.
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 2026.10.19-9814e911.
AtlasHvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørSekvenser genomet ditt↗
From traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
Fra 449 $
Gratis frakt · Resultater på 6–8 uker
