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Tunnus
Abnormal feet structure
Kliiniline nimetus: Abnormal foot morphology
An abnormality of the skeleton of foot.
Kokkuvõte
- Teised nimetused
- Abnormality of the feet, Abnormality of the foot, Foot deformities, Foot deformity
- Kehasüsteem
- Abnormality of limbs
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Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/abnormal-foot-morphology.json"
page <- fromJSON(url)
page$trait$nameAbnormal feet structureHP:0001760
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Logi sisseKüsiSekveneeri oma genoom↗
Lugege välja geenid, mis on seotud Abnormal feet structure-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test72 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.
- Fanconi AnemiaReads 18 of these genesBRCA1BRCA2BRIP1ERCC4FANCAFANCBAbout this report →
- DNA Repair DiseaseReads 18 of these genesBRCA1BRCA2BRIP1ERCC4FANCAFANCBAbout this report →
- Ehlers-Danlos SyndromeReads 10 of these genesAEBP1TNXBCHST14COL1A1COL1A2DSEAbout this report →
- Charcot-Marie-Tooth DiseaseReads 14 of these genesGDAP1HK1LMNAMFN2NEFLSBF2About this report →
Show 68 more reports
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesBRIP1PALB2RAD51CAbout this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 2 of these genesTREM2TYROBPAbout this report →
- Alkuraya-Kucinskas SyndromeReads 1 of these genesBLTP1About this report →
- Caffey DiseaseReads 1 of these genesCOL1A1About this report →
- Christianson SyndromeReads 1 of these genesSLC9A6About this report →
- CHRNG-Related Multiple Pterygium SyndromeReads 1 of these genesCHRNGAbout this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- FAT4-Related Neurodevelopmental DisorderReads 1 of these genesFAT4About this report →
- Friedreich AtaxiaReads 1 of these genesFXNAbout this report →
- HypophosphatasiaReads 1 of these genesALPLAbout this report →
- Miller Syndrome (Postaxial Acrofacial Dysostosis)Reads 1 of these genesDHODHAbout this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- Progressive Pseudorheumatoid DysplasiaReads 1 of these genesCCN6About this report →
- Salla Disease and Free Sialic Acid Storage DiseaseReads 1 of these genesSLC17A5About this report →
- Snijders Blok-Campeau SyndromeReads 1 of these genesCHD3About this report →
- Townes-Brocks SyndromeReads 1 of these genesSALL1About this report →
- TRPV4-Related Skeletal DysplasiasReads 1 of these genesTRPV4About this report →
- Rare Hereditary Peripheral NeuropathiesReads 15 of these genesGDAP1HK1LMNAMFN2NEFLPEX7About this report →
- Inherited Neurodegenerative DisordersReads 16 of these genesPEX7FXNLETM1SPARTALDH3A2ASAH1About this report →
- Spinal Muscular AtrophyReads 4 of these genesASAH1DYNC1H1EXOSC3VRK1About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 3 of these genesADAMTS3CCBE1FAT4About this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A24About this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Intellectual DisabilityReads 9 of these genesDYRK1ANSD2PIGGRAI1AUTS2MED13LAbout this report →
- LipodystrophyReads 2 of these genesLMNAMFN2About this report →
- Achondrogenesis panelReads 1 of these genesCOL2A1About this report →
- Other Inherited LeukodystrophiesReads 4 of these genesPEX7ALDH3A2TREM2TYROBPAbout this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGAPIGGAbout this report →
- Alzheimer diseaseReads 1 of these genesTREM2About this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 2 of these genesEXOSC3VRK1About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 1 of these genesPHYHAbout this report →
- Congenital Disorders of GlycosylationReads 4 of these genesPIGACHST14DSEPIGGAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 3 of these genesFXNSACSTMEM216About this report →
- VitreoretinopathyReads 2 of these genesCOL2A1DYNC1H1About this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesPORAbout this report →
- Hereditary Spastic ParaplegiaReads 3 of these genesSPARTATP13A2ERLIN2About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Pyruvate Kinase Deficiency and Other Red Cell Enzyme DisordersReads 1 of these genesHK1About this report →
- Osteogenesis ImperfectaReads 2 of these genesCOL1A1COL1A2About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 2 of these genesSLURP1GJB6About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesCOL2A1About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesATP13A2About this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 1 of these genesSLC18A2About this report →
- HyperinsulinismReads 1 of these genesHK1About this report →
- Usher SyndromeReads 1 of these genesHARS1About this report →
- Frontotemporal DementiaReads 1 of these genesHNRNPA1About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesATP13A2About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX7About this report →
- Lysosomal Storage DiseaseReads 2 of these genesASAH1SLC17A5About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesDYNC1H1About this report →
- Parkinson DiseaseReads 1 of these genesATP13A2About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesCPT2About this report →
- Ectodermal DysplasiasReads 1 of these genesGJB6About this report →
- Distal MyopathiesReads 1 of these genesHNRNPA1About this report →
- Autoimmune DiseaseReads 1 of these genesCHRNGAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesPORAbout this report →
- Hearing Loss and DeafnessReads 2 of these genesMYH14GJB6About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesMYO9AAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesHNRNPA1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSLC18A2About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesTMEM216About this report →
- Male InfertilityReads 1 of these genesFANCMAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesPIGACPLX1About this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Female InfertilityReads 1 of these genesFANCMAbout this report →
- Retinitis PigmentosaReads 1 of these genesHK1About this report →
Lugege välja geenid, mis on seotud Abnormal feet structure-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test102 geeni on seotud tunnusega Abnormal feet structure
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Abnormal feet structure. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Alati | Esineb 1 haiguses |
| TAF2TATA-box binding protein associated factor 2 | Alati | Esineb 2 haiguses |
| AEBP1AE binding protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GDAP1ganglioside induced differentiation associated protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| HK1hexokinase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LMNAlamin A/C | Väga sageli (80–99%) | Esineb 2 haiguses |
| MFN2mitofusin 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NEFLneurofilament light chain | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX7peroxisomal biogenesis factor 7 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PHYHphytanoyl-CoA 2-hydroxylase | Väga sageli (80–99%) | Esineb 1 haiguses |
| SBF2SET binding factor 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC18A2solute carrier family 18 member A2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC25A24solute carrier family 25 member 24 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLURP1secreted LY6/PLAUR domain containing 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TNXBtenascin XB | Väga sageli (80–99%) | Esineb 1 haiguses |
| CHRNGcholinergic receptor nicotinic gamma subunit | Sageli (30–79%) | Esineb 1 haiguses |
| CHST14carbohydrate sulfotransferase 14 | Sageli (30–79%) | Esineb 1 haiguses |
| COL1A1collagen type I alpha 1 chain | Sageli (30–79%) | Esineb 2 haiguses |
| COL1A2collagen type I alpha 2 chain | Sageli (30–79%) | Esineb 1 haiguses |
| CPLX1complexin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CTBP1C-terminal binding protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DACT1dishevelled binding antagonist of beta catenin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DSEdermatan sulfate epimerase | Sageli (30–79%) | Esineb 1 haiguses |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Sageli (30–79%) | Esineb 1 haiguses |
| FXNfrataxin | Sageli (30–79%) | Esineb 1 haiguses |
| HARS1histidyl-tRNA synthetase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| HINT1histidine triad nucleotide binding protein 1 | Sageli (30–79%) | Esineb 2 haiguses |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MYH14myosin heavy chain 14 | Sageli (30–79%) | Esineb 1 haiguses |
| MYH3myosin heavy chain 3 | Sageli (30–79%) | Esineb 1 haiguses |
| NDRG1N-myc downstream regulated 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NELFAnegative elongation factor complex member A | Sageli (30–79%) | Esineb 1 haiguses |
| NSD2nuclear receptor binding SET domain protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Sageli (30–79%) | Esineb 1 haiguses |
| PRDM5PR/SET domain 5 | Sageli (30–79%) | Esineb 1 haiguses |
| PTRH2peptidyl-tRNA hydrolase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| RAI1retinoic acid induced 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SALL1spalt like transcription factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SPARTspartin | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 62 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| ZNF469zinc finger protein 469 | Sageli (30–79%) | Esineb 1 haiguses |
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ASAH1N-acylsphingosine amidohydrolase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP13A2ATPase cation transporting 13A2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| AUTS2activator of transcription and developmental regulator AUTS2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRCA1BRCA1 DNA repair associated | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRCA2BRCA2 DNA repair associated | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRIP1BRCA1 interacting DNA helicase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CCBE1collagen and calcium binding EGF domains 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL2A1collagen type II alpha 1 chain | Mõnikord (5–29%) | Esineb 2 haiguses |
| COL5A1collagen type V alpha 1 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL5A2collagen type V alpha 2 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERLIN2ER lipid raft associated 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FAAP100FA core complex associated protein 100 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCAFA complementation group A | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCBFA complementation group B | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCCFA complementation group C | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCD2FA complementation group D2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCEFA complementation group E | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCFFA complementation group F | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCGFA complementation group G | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCIFA complementation group I | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCLFA complementation group L | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCMFA complementation group M | Mõnikord (5–29%) | Esineb 1 haiguses |
| FAT4FAT atypical cadherin 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAD2L2mitotic arrest deficient 2 like 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MED13Lmediator complex subunit 13L | Mõnikord (5–29%) | Esineb 1 haiguses |
| NEK9NIMA related kinase 9 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PALB2partner and localizer of BRCA2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PORcytochrome p450 oxidoreductase | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAD51RAD51 recombinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAD51CRAD51 paralog C | Mõnikord (5–29%) | Esineb 1 haiguses |
| RFWD3ring finger and WD repeat domain 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SACSsacsin molecular chaperone | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLX4SLX4 structure-specific endonuclease subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| UBE2Tubiquitin conjugating enzyme E2 T | Mõnikord (5–29%) | Esineb 1 haiguses |
| XRCC2X-ray repair cross complementing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALPLalkaline phosphatase, biomineralization associated | Pole registreeritud | Esineb 1 haiguses |
| BLTP1bridge-like lipid transfer protein family member 1 | Pole registreeritud | Esineb 1 haiguses |
| CCN6cellular communication network factor 6 | Pole registreeritud | Esineb 1 haiguses |
| CCT5chaperonin containing TCP1 subunit 5 | Pole registreeritud | Esineb 1 haiguses |
| CHD3chromodomain helicase DNA binding protein 3 | Pole registreeritud | Esineb 1 haiguses |
| CNTNAP1contactin associated protein 1 | Pole registreeritud | Esineb 1 haiguses |
| CPT2carnitine palmitoyltransferase 2 | Pole registreeritud | Esineb 1 haiguses |
| DCHS1dachsous cadherin-related 1 | Pole registreeritud | Esineb 1 haiguses |
| DHODHdihydroorotate dehydrogenase (quinone) | Pole registreeritud | Esineb 1 haiguses |
| DYNC1H1dynein cytoplasmic 1 heavy chain 1 | Pole registreeritud | Esineb 1 haiguses |
| EXOSC3exosome component 3 | Pole registreeritud | Esineb 1 haiguses |
| GJB6gap junction protein beta 6 | Pole registreeritud | Esineb 1 haiguses |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Pole registreeritud | Esineb 1 haiguses |
| MYO9Amyosin IXA | Pole registreeritud | Esineb 1 haiguses |
| SLC17A5solute carrier family 17 member 5 | Pole registreeritud | Esineb 1 haiguses |
| SLC9A6solute carrier family 9 member A6 | Pole registreeritud | Esineb 1 haiguses |
| SYT1synaptotagmin 1 | Pole registreeritud | Esineb 1 haiguses |
| TMEM216transmembrane protein 216 | Pole registreeritud | Esineb 1 haiguses |
| TREM2triggering receptor expressed on myeloid cells 2 | Pole registreeritud | Esineb 1 haiguses |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Pole registreeritud | Esineb 1 haiguses |
| TYROBPtransmembrane immune signaling adaptor TYROBP | Pole registreeritud | Esineb 1 haiguses |
| VRK1VRK serine/threonine kinase 1 | Pole registreeritud | Esineb 1 haiguses |
| YARS1tyrosyl-tRNA synthetase 1 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Kitsamad tunnused
- Dropped arches397 geeni
- High-arched foot315 geeni
- Broad foot40 geeni
- Long foot27 geeni
- Contractures of the foot joints18 geeni
- Split foot14 geeni
- Abnormalities of the toes11 geeni
- Abnormality of the Achilles tendon9 geeni
- Abnormality of the long bone of foot9 geeni
- Positional foot deformity7 geeni
- Narrow foot6 geeni
- Structural foot deformity4 geeni
- Abnormal ankle bones3 geeni
- Foot bone infection3 geeni
- Abnormal foot bone ossification2 geeni
- Abnormality of the plantar skin of foot2 geeni
- Autoamputation of foot2 geeni
- Ankylosis of feet small joints1 geen
- Medial deviation of the foot1 geen
- Medial rotation of the medial malleolus1 geen
- Osteolysis involving bones of the feet1 geen
- Podagra1 geen
- Prominent subcalcaneal fat pad1 geen
- Absent/small foot bones
- Duplication involving bones of the feet
- Fusion involving the bones of the feet
- Hindfoot deformity
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.19-9814e911.
AtlasKellele me abi osutameMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
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.
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Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
