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Kirjaudu sisäänKysySekvensoi genomisi↗
Piirre
Abnormality of the nail
Kliininen nimi: Abnormal nail morphology
Abnormal structure or appearance of the nail.
Yhteenveto
- Tunnetaan myös nimellä
- Nail disease
- Elimistön järjestelmä
- Abnormality of the integument
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-nail-morphology.json"
page <- fromJSON(url)
page$trait$nameAbnormality of the nailHP:0001597
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Lue Abnormality of the nail-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test63 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.
- Inherited IchthyosesReads 11 of these genesABCA12ALOX12BALOXE3CERS3KRT1NIPAL4About this report →
- Multiple Synostoses Syndrome (FGF9)Reads 4 of these genesFGF9GDF5GDF6NOGAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 11 of these genesGJA1CTSCDSG1DSPKRT1MBTPS2About this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 7 of these genesDSG4KRT81KRT83KRT86HRCDSNAbout this report →
Show 59 more reports
- Chronic Mucocutaneous CandidiasisReads 3 of these genesIL17RAIL17RCTRAF3IP2About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 2 of these genesPDE4DPRKAR1AAbout this report →
- ACAN-Related Short StatureReads 1 of these genesACANAbout this report →
- AlkaptonuriaReads 1 of these genesHGDAbout this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
- Johanson-Blizzard SyndromeReads 1 of these genesUBR1About this report →
- MEND SyndromeReads 1 of these genesEBPAbout this report →
- Nail-Patella SyndromeReads 1 of these genesLMX1BAbout this report →
- NOG-Related Symphalangism Spectrum DisorderReads 1 of these genesNOGAbout this report →
- Epidermolysis BullosaReads 4 of these genesLAMC2LAMA3LAMB3DSPAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 2 of these genesCYB5ACYB5R3About this report →
- Hereditary Orofacial CleftingReads 2 of these genesMSX1IRF6About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 2 of these genesEVCEVC2About this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 2 of these genesCASRGNA11About this report →
- Acrodermatitis EnteropathicaReads 1 of these genesSLC39A4About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesAKT1About this report →
- Darier and Hailey-Hailey DiseaseReads 1 of these genesATP2A2About this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A24About this report →
- TyrosinemiaReads 1 of these genesTATAbout this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesIRF6About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 3 of these genesCOX7BHCCSNDUFB11About this report →
- Achondrogenesis panelReads 1 of these genesGDF5About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Amelogenesis ImperfectaReads 2 of these genesLAMB3DLX3About this report →
- Ectodermal DysplasiasReads 2 of these genesTP63LEF1About this report →
- Autoimmune DiseaseReads 2 of these genesCTLA4TREX1About this report →
- Systemic Lupus ErythematosusReads 1 of these genesTREX1About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesFUCA1About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesCTLA4About this report →
- Hypodontia and AnodontiaReads 1 of these genesMSX1About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesCTLA4About this report →
- Thyroid CancerReads 2 of these genesCASRGNA11About this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesTREX1About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 2 of these genesIL36RNTREX1About this report →
- Other Inborn Errors of ImmunityReads 5 of these genesIL17RAIL17RCTRAF3IP2CTLA4TREX1About this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesDSPAbout this report →
- Polycystic Kidney DiseaseReads 1 of these genesIFT140About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Type I InterferonopathiesReads 1 of these genesTREX1About this report →
- OsteopetrosisReads 1 of these genesCTSKAbout this report →
- Lysosomal Storage DiseaseReads 2 of these genesCTSKFUCA1About this report →
- Congenital MyopathiesReads 1 of these genesMAP3K20About this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR2About this report →
- Inherited ThrombocytopeniasReads 1 of these genesKDSRAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesMBTPS2About this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Female InfertilityReads 1 of these genesTP63About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesTREX1About this report →
- Retinitis PigmentosaReads 1 of these genesIFT140About this report →
- Hearing Loss and DeafnessReads 1 of these genesGJB2About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesNDUFB11About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesLMNAAbout this report →
- Intellectual DisabilityReads 1 of these genesADNPAbout this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesTREX1About this report →
Lue Abnormality of the nail-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test85 geeniä, jotka liittyvät piirteeseen Abnormality of the nail
Näiden geenien muutokset aiheuttavat harvinaisia sairauksia, joissa Abnormality of the nail 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 |
|---|---|---|
| LAMC2laminin subunit gamma 2 | Aina | 2 sairaudessa |
| ACANaggrecan | Hyvin usein (80–99%) | 1 sairaudessa |
| AP1S3adaptor related protein complex 1 subunit sigma 3 | Hyvin usein (80–99%) | 1 sairaudessa |
| ATP2A2ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 | Hyvin usein (80–99%) | 1 sairaudessa |
| CLEC7AC-type lectin domain containing 7A | Hyvin usein (80–99%) | 1 sairaudessa |
| DSG4desmoglein 4 | Hyvin usein (80–99%) | 1 sairaudessa |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| EVCEvC ciliary complex subunit 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| EVC2EvC ciliary complex subunit 2 | Hyvin usein (80–99%) | 1 sairaudessa |
| GJA1gap junction protein alpha 1 | Hyvin usein (80–99%) | 3 sairaudessa |
| GLI1GLI family zinc finger 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| HLA-Bmajor histocompatibility complex, class I, B | Hyvin usein (80–99%) | 1 sairaudessa |
| IL17Finterleukin 17F | Hyvin usein (80–99%) | 1 sairaudessa |
| IL17RAinterleukin 17 receptor A | Hyvin usein (80–99%) | 1 sairaudessa |
| IL17RCinterleukin 17 receptor C | Hyvin usein (80–99%) | 1 sairaudessa |
| IL36RNinterleukin 36 receptor antagonist | Hyvin usein (80–99%) | 1 sairaudessa |
| KRT81keratin 81 | Hyvin usein (80–99%) | 1 sairaudessa |
| KRT83keratin 83 | Hyvin usein (80–99%) | 1 sairaudessa |
| KRT86keratin 86 | Hyvin usein (80–99%) | 1 sairaudessa |
| LAMA3laminin subunit alpha 3 | Hyvin usein (80–99%) | 1 sairaudessa |
| LAMB3laminin subunit beta 3 | Hyvin usein (80–99%) | 1 sairaudessa |
| LMX1BLIM homeobox transcription factor 1 beta | Hyvin usein (80–99%) | 1 sairaudessa |
| MSX1msh homeobox 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| PDE4Dphosphodiesterase 4D | Hyvin usein (80–99%) | 1 sairaudessa |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Hyvin usein (80–99%) | 1 sairaudessa |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Hyvin usein (80–99%) | 1 sairaudessa |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Hyvin usein (80–99%) | 1 sairaudessa |
| SLC25A24solute carrier family 25 member 24 | Hyvin usein (80–99%) | 1 sairaudessa |
| SMARCAD1SNF2 related chromatin remodeling ATPase with DExD box 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| TP63tumor protein p63 | Hyvin usein (80–99%) | 1 sairaudessa |
| TRAF3IP2TRAF3 interacting protein 2 | Hyvin usein (80–99%) | 1 sairaudessa |
| ABCA12ATP binding cassette subfamily A member 12 | Usein (30–79%) | 1 sairaudessa |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Usein (30–79%) | 1 sairaudessa |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Usein (30–79%) | 1 sairaudessa |
| CARD14caspase recruitment domain family member 14 | Usein (30–79%) | 1 sairaudessa |
| CASRcalcium sensing receptor | Usein (30–79%) | 1 sairaudessa |
| CERS3ceramide synthase 3 | Usein (30–79%) | 1 sairaudessa |
| CTSCcathepsin C | Usein (30–79%) | 1 sairaudessa |
| CTSKcathepsin K | Usein (30–79%) | 1 sairaudessa |
| CYB5Acytochrome b5 type A | Usein (30–79%) | 1 sairaudessa |
Näytä 45 geeniä lisää
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| CYB5R3cytochrome b5 reductase 3 | Usein (30–79%) | 1 sairaudessa |
| DLX3distal-less homeobox 3 | Usein (30–79%) | 1 sairaudessa |
| DSG1desmoglein 1 | Usein (30–79%) | 1 sairaudessa |
| DSPdesmoplakin | Usein (30–79%) | 1 sairaudessa |
| GNA11G protein subunit alpha 11 | Usein (30–79%) | 1 sairaudessa |
| HGDhomogentisate 1,2-dioxygenase | Usein (30–79%) | 1 sairaudessa |
| IFT140intraflagellar transport 140 | Usein (30–79%) | 1 sairaudessa |
| IRF6interferon regulatory factor 6 | Usein (30–79%) | 1 sairaudessa |
| KRT1keratin 1 | Usein (30–79%) | 1 sairaudessa |
| LMNAlamin A/C | Usein (30–79%) | 2 sairaudessa |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Usein (30–79%) | 1 sairaudessa |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Usein (30–79%) | 1 sairaudessa |
| NIPAL4NIPA like domain containing 4 | Usein (30–79%) | 1 sairaudessa |
| PNPLA1patatin like domain 1, omega-hydroxyceramide transacylase | Usein (30–79%) | 1 sairaudessa |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Usein (30–79%) | 1 sairaudessa |
| SLC39A4solute carrier family 39 member 4 | Usein (30–79%) | 1 sairaudessa |
| SULT2B1sulfotransferase family 2B member 1 | Usein (30–79%) | 1 sairaudessa |
| TGM1transglutaminase 1 | Usein (30–79%) | 1 sairaudessa |
| ADNPactivity dependent neuroprotector homeobox | Joskus (5–29%) | 1 sairaudessa |
| AKT1AKT serine/threonine kinase 1 | Joskus (5–29%) | 1 sairaudessa |
| CD28CD28 molecule | Joskus (5–29%) | 1 sairaudessa |
| COX7Bcytochrome c oxidase subunit 7B | Joskus (5–29%) | 1 sairaudessa |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Joskus (5–29%) | 1 sairaudessa |
| EBPEBP cholestenol delta-isomerase | Joskus (5–29%) | 1 sairaudessa |
| FBXO22F-box protein 22 | Joskus (5–29%) | 1 sairaudessa |
| FGF9fibroblast growth factor 9 | Joskus (5–29%) | 1 sairaudessa |
| FGFR2fibroblast growth factor receptor 2 | Joskus (5–29%) | 1 sairaudessa |
| FUCA1alpha-L-fucosidase 1 | Joskus (5–29%) | 1 sairaudessa |
| GDF5growth differentiation factor 5 | Joskus (5–29%) | 1 sairaudessa |
| GDF6growth differentiation factor 6 | Joskus (5–29%) | 1 sairaudessa |
| GJB2gap junction protein beta 2 | Joskus (5–29%) | 1 sairaudessa |
| GJB3gap junction protein beta 3 | Joskus (5–29%) | 1 sairaudessa |
| GJB4gap junction protein beta 4 | Joskus (5–29%) | 1 sairaudessa |
| HCCSholocytochrome c synthase | Joskus (5–29%) | 1 sairaudessa |
| HRHR lysine demethylase and nuclear receptor corepressor | Joskus (5–29%) | 1 sairaudessa |
| KDSR3-ketodihydrosphingosine reductase | Joskus (5–29%) | 1 sairaudessa |
| LEF1lymphoid enhancer binding factor 1 | Joskus (5–29%) | 1 sairaudessa |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Joskus (5–29%) | 1 sairaudessa |
| NOGnoggin | Joskus (5–29%) | 1 sairaudessa |
| TATtyrosine aminotransferase | Joskus (5–29%) | 1 sairaudessa |
| TNFRSF1BTNF receptor superfamily member 1B | Joskus (5–29%) | 1 sairaudessa |
| TREX1three prime repair exonuclease 1 | Joskus (5–29%) | 1 sairaudessa |
| CDSNcorneodesmosin | Ei kirjattu | 1 sairaudessa |
| KRT74keratin 74 | Ei kirjattu | 1 sairaudessa |
| UBR1ubiquitin protein ligase E3 component n-recognin 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
- Poor nail formation130 geeniä
- Abnormal fingernails99 geeniä
- Atypical nail growth84 geeniä
- Brittle nails35 geeniä
- Abnormality of the toenail33 geeniä
- Thick nail19 geeniä
- Absent/small nails16 geeniä
- Thin nail16 geeniä
- Abnormal periungual morphology3 geeniä
- Abnormality of nail color3 geeniä
- Nailfold capillary tortuosity3 geeniä
- Chronic monilial nail infection2 geeniä
- Nail bed hemorrhage2 geeniä
- Nail bed telangiectasia2 geeniä
- Abnormal subungual morphology1 geeni
- Longitudinal erythronychia1 geeni
- Onychoheterotopia1 geeni
- Pyramidal skinfold extending from the base to the top of the nails1 geeni
- Splinter hemorrhages1 geeni
- Abnormal nail attachment
- Abnormal nail growth
- Abnormal nail surface
- Nail tumor
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.
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