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Piirre
Abnormal feet structure
Kliininen nimi: Abnormal foot morphology
An abnormality of the skeleton of foot.
Yhteenveto
- Tunnetaan myös nimellä
- Abnormality of the feet, Abnormality of the foot, Foot deformities, Foot deformity
- Elimistön järjestelmä
- Abnormality of limbs
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Tämä sivu datana
Lisää sivun osoitteen perään .json tai pyydä application/json-muotoa, niin saat sivun JSON-muodossa.
library(jsonlite)
url <- "https://dantelabs.com/traits/abnormal-foot-morphology.json"
page <- fromJSON(url)
page$trait$nameAbnormal feet structureHP:0001760
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Lue Abnormal feet structure-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
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Tilaa 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 →
Lue Abnormal feet structure-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
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Tilaa Genome Test102 geeniä, jotka liittyvät piirteeseen Abnormal feet structure
Näiden geenien muutokset aiheuttavat harvinaisia sairauksia, joissa Abnormal feet structure esiintyy. Useimmilla, joilla on tämä piirre, ei ole mitään näistä sairauksista, eikä tämän listan geeni kerro mitään kenenkään omasta genomista.
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Aina | 1 sairaudessa |
| TAF2TATA-box binding protein associated factor 2 | Aina | 2 sairaudessa |
| AEBP1AE binding protein 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| GDAP1ganglioside induced differentiation associated protein 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| HK1hexokinase 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| LMNAlamin A/C | Hyvin usein (80–99%) | 2 sairaudessa |
| MFN2mitofusin 2 | Hyvin usein (80–99%) | 1 sairaudessa |
| NEFLneurofilament light chain | Hyvin usein (80–99%) | 1 sairaudessa |
| PEX7peroxisomal biogenesis factor 7 | Hyvin usein (80–99%) | 1 sairaudessa |
| PHYHphytanoyl-CoA 2-hydroxylase | Hyvin usein (80–99%) | 1 sairaudessa |
| SBF2SET binding factor 2 | Hyvin usein (80–99%) | 1 sairaudessa |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Hyvin usein (80–99%) | 1 sairaudessa |
| SLC18A2solute carrier family 18 member A2 | Hyvin usein (80–99%) | 1 sairaudessa |
| SLC25A24solute carrier family 25 member 24 | Hyvin usein (80–99%) | 1 sairaudessa |
| SLURP1secreted LY6/PLAUR domain containing 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| TNXBtenascin XB | Hyvin usein (80–99%) | 1 sairaudessa |
| CHRNGcholinergic receptor nicotinic gamma subunit | Usein (30–79%) | 1 sairaudessa |
| CHST14carbohydrate sulfotransferase 14 | Usein (30–79%) | 1 sairaudessa |
| COL1A1collagen type I alpha 1 chain | Usein (30–79%) | 2 sairaudessa |
| COL1A2collagen type I alpha 2 chain | Usein (30–79%) | 1 sairaudessa |
| CPLX1complexin 1 | Usein (30–79%) | 1 sairaudessa |
| CTBP1C-terminal binding protein 1 | Usein (30–79%) | 1 sairaudessa |
| DACT1dishevelled binding antagonist of beta catenin 1 | Usein (30–79%) | 1 sairaudessa |
| DSEdermatan sulfate epimerase | Usein (30–79%) | 1 sairaudessa |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Usein (30–79%) | 1 sairaudessa |
| FXNfrataxin | Usein (30–79%) | 1 sairaudessa |
| HARS1histidyl-tRNA synthetase 1 | Usein (30–79%) | 1 sairaudessa |
| HINT1histidine triad nucleotide binding protein 1 | Usein (30–79%) | 2 sairaudessa |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Usein (30–79%) | 1 sairaudessa |
| MYH14myosin heavy chain 14 | Usein (30–79%) | 1 sairaudessa |
| MYH3myosin heavy chain 3 | Usein (30–79%) | 1 sairaudessa |
| NDRG1N-myc downstream regulated 1 | Usein (30–79%) | 1 sairaudessa |
| NELFAnegative elongation factor complex member A | Usein (30–79%) | 1 sairaudessa |
| NSD2nuclear receptor binding SET domain protein 2 | Usein (30–79%) | 1 sairaudessa |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Usein (30–79%) | 1 sairaudessa |
| PRDM5PR/SET domain 5 | Usein (30–79%) | 1 sairaudessa |
| PTRH2peptidyl-tRNA hydrolase 2 | Usein (30–79%) | 1 sairaudessa |
| RAI1retinoic acid induced 1 | Usein (30–79%) | 1 sairaudessa |
| SALL1spalt like transcription factor 1 | Usein (30–79%) | 1 sairaudessa |
| SPARTspartin | Usein (30–79%) | 1 sairaudessa |
Näytä 62 geeniä lisää
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| ZNF469zinc finger protein 469 | Usein (30–79%) | 1 sairaudessa |
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Joskus (5–29%) | 1 sairaudessa |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Joskus (5–29%) | 1 sairaudessa |
| ASAH1N-acylsphingosine amidohydrolase 1 | Joskus (5–29%) | 1 sairaudessa |
| ATP13A2ATPase cation transporting 13A2 | Joskus (5–29%) | 1 sairaudessa |
| AUTS2activator of transcription and developmental regulator AUTS2 | Joskus (5–29%) | 1 sairaudessa |
| BRCA1BRCA1 DNA repair associated | Joskus (5–29%) | 1 sairaudessa |
| BRCA2BRCA2 DNA repair associated | Joskus (5–29%) | 1 sairaudessa |
| BRIP1BRCA1 interacting DNA helicase 1 | Joskus (5–29%) | 1 sairaudessa |
| CCBE1collagen and calcium binding EGF domains 1 | Joskus (5–29%) | 1 sairaudessa |
| COL2A1collagen type II alpha 1 chain | Joskus (5–29%) | 2 sairaudessa |
| COL5A1collagen type V alpha 1 chain | Joskus (5–29%) | 1 sairaudessa |
| COL5A2collagen type V alpha 2 chain | Joskus (5–29%) | 1 sairaudessa |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Joskus (5–29%) | 1 sairaudessa |
| ERLIN2ER lipid raft associated 2 | Joskus (5–29%) | 1 sairaudessa |
| FAAP100FA core complex associated protein 100 | Joskus (5–29%) | 1 sairaudessa |
| FANCAFA complementation group A | Joskus (5–29%) | 1 sairaudessa |
| FANCBFA complementation group B | Joskus (5–29%) | 1 sairaudessa |
| FANCCFA complementation group C | Joskus (5–29%) | 1 sairaudessa |
| FANCD2FA complementation group D2 | Joskus (5–29%) | 1 sairaudessa |
| FANCEFA complementation group E | Joskus (5–29%) | 1 sairaudessa |
| FANCFFA complementation group F | Joskus (5–29%) | 1 sairaudessa |
| FANCGFA complementation group G | Joskus (5–29%) | 1 sairaudessa |
| FANCIFA complementation group I | Joskus (5–29%) | 1 sairaudessa |
| FANCLFA complementation group L | Joskus (5–29%) | 1 sairaudessa |
| FANCMFA complementation group M | Joskus (5–29%) | 1 sairaudessa |
| FAT4FAT atypical cadherin 4 | Joskus (5–29%) | 1 sairaudessa |
| MAD2L2mitotic arrest deficient 2 like 2 | Joskus (5–29%) | 1 sairaudessa |
| MED13Lmediator complex subunit 13L | Joskus (5–29%) | 1 sairaudessa |
| NEK9NIMA related kinase 9 | Joskus (5–29%) | 1 sairaudessa |
| PALB2partner and localizer of BRCA2 | Joskus (5–29%) | 1 sairaudessa |
| PORcytochrome p450 oxidoreductase | Joskus (5–29%) | 1 sairaudessa |
| RAD51RAD51 recombinase | Joskus (5–29%) | 1 sairaudessa |
| RAD51CRAD51 paralog C | Joskus (5–29%) | 1 sairaudessa |
| RFWD3ring finger and WD repeat domain 3 | Joskus (5–29%) | 1 sairaudessa |
| SACSsacsin molecular chaperone | Joskus (5–29%) | 1 sairaudessa |
| SLX4SLX4 structure-specific endonuclease subunit | Joskus (5–29%) | 1 sairaudessa |
| UBE2Tubiquitin conjugating enzyme E2 T | Joskus (5–29%) | 1 sairaudessa |
| XRCC2X-ray repair cross complementing 2 | Joskus (5–29%) | 1 sairaudessa |
| ALPLalkaline phosphatase, biomineralization associated | Ei kirjattu | 1 sairaudessa |
| BLTP1bridge-like lipid transfer protein family member 1 | Ei kirjattu | 1 sairaudessa |
| CCN6cellular communication network factor 6 | Ei kirjattu | 1 sairaudessa |
| CCT5chaperonin containing TCP1 subunit 5 | Ei kirjattu | 1 sairaudessa |
| CHD3chromodomain helicase DNA binding protein 3 | Ei kirjattu | 1 sairaudessa |
| CNTNAP1contactin associated protein 1 | Ei kirjattu | 1 sairaudessa |
| CPT2carnitine palmitoyltransferase 2 | Ei kirjattu | 1 sairaudessa |
| DCHS1dachsous cadherin-related 1 | Ei kirjattu | 1 sairaudessa |
| DHODHdihydroorotate dehydrogenase (quinone) | Ei kirjattu | 1 sairaudessa |
| DYNC1H1dynein cytoplasmic 1 heavy chain 1 | Ei kirjattu | 1 sairaudessa |
| EXOSC3exosome component 3 | Ei kirjattu | 1 sairaudessa |
| GJB6gap junction protein beta 6 | Ei kirjattu | 1 sairaudessa |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Ei kirjattu | 1 sairaudessa |
| MYO9Amyosin IXA | Ei kirjattu | 1 sairaudessa |
| SLC17A5solute carrier family 17 member 5 | Ei kirjattu | 1 sairaudessa |
| SLC9A6solute carrier family 9 member A6 | Ei kirjattu | 1 sairaudessa |
| SYT1synaptotagmin 1 | Ei kirjattu | 1 sairaudessa |
| TMEM216transmembrane protein 216 | Ei kirjattu | 1 sairaudessa |
| TREM2triggering receptor expressed on myeloid cells 2 | Ei kirjattu | 1 sairaudessa |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Ei kirjattu | 1 sairaudessa |
| TYROBPtransmembrane immune signaling adaptor TYROBP | Ei kirjattu | 1 sairaudessa |
| VRK1VRK serine/threonine kinase 1 | Ei kirjattu | 1 sairaudessa |
| YARS1tyrosyl-tRNA synthetase 1 | Ei kirjattu | 1 sairaudessa |
Kuinka usein ilmiö esiintyy ihmisillä, joilla on jokin geenin sairauksista, niin kuin Human Phenotype Ontology sen kirjaa. Nämä sivut kuvaavat piirteitä ja niiden taustalla olevaa tutkimusta, eivätkä ne ole diagnoosi. Oireista kannattaa kysyä lääkäriltä tai geneettiseltä neuvojalta.
Tarkemmat piirteet
- Dropped arches397 geeniä
- High-arched foot315 geeniä
- Broad foot40 geeniä
- Long foot27 geeniä
- Contractures of the foot joints18 geeniä
- Split foot14 geeniä
- Abnormalities of the toes11 geeniä
- Abnormality of the Achilles tendon9 geeniä
- Abnormality of the long bone of foot9 geeniä
- Positional foot deformity7 geeniä
- Narrow foot6 geeniä
- Structural foot deformity4 geeniä
- Abnormal ankle bones3 geeniä
- Foot bone infection3 geeniä
- Abnormal foot bone ossification2 geeniä
- Abnormality of the plantar skin of foot2 geeniä
- Autoamputation of foot2 geeniä
- Ankylosis of feet small joints1 geeni
- Medial deviation of the foot1 geeni
- Medial rotation of the medial malleolus1 geeni
- Osteolysis involving bones of the feet1 geeni
- Podagra1 geeni
- Prominent subcalcaneal fat pad1 geeni
- Absent/small foot bones
- Duplication involving bones of the feet
- Fusion involving the bones of the feet
- Hindfoot deformity
Laajemmat piirteet
Mistä tämä tieto tulee
- Human Phenotype Ontology, julkaisu 2026-09-01: piirre, sen nimet, määritelmä ja siihen liitetyt geenit. Lue lisää osoitteesta hpo.jax.org.
- Tietojulkaisu 2026.10.19-9814e911.
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
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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