AtlasPožymis
Small fingernail
Klinikinis pavadinimas: Hypoplastic fingernail
Underdevelopment of a fingernail.
Santrauka
- Taip pat vadinama
- Underdeveloped fingernail
- Kūno sistema
- Abnormality of the integument
AtlasŠi puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/hypoplastic-fingernail.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Small fingernail, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test27 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.
- Adams-Oliver SyndromeReads 6 of these genesARHGAP31DLL4DOCK6EOGTNOTCH1RBPJAbout this report →
- DOORS SyndromeReads 2 of these genesTBC1D24ATP6V1B2About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 4 of these genesCDKN1CHMGA2IGF2PLAG1About this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
Show 23 more reports
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- KCNH1-Related DisorderReads 1 of these genesKCNH1About this report →
- PLEC-Related Epidermolysis Bullosa and Muscular DystrophyReads 1 of these genesPLECAbout this report →
- SHOX Deficiency (Leri-Weill and Langer Dysplasia)Reads 1 of these genesSHOXAbout this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL11A2About this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGOPIGNAbout this report →
- Syndromic CraniosynostosisReads 2 of these genesFGFR2ZNF462About this report →
- Hereditary Orofacial CleftingReads 1 of these genesMSX1About this report →
- Hypodontia and AnodontiaReads 1 of these genesMSX1About this report →
- Hearing Loss and DeafnessReads 3 of these genesTBC1D24COL11A1COL11A2About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesNOTCH1About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesCDKN1CIGF2About this report →
- Epidermolysis BullosaReads 1 of these genesPLECAbout this report →
- Epilepsy (Full Panel)Reads 3 of these genesFBXO28TBC1D24ATP6V1B2About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesPIGOPIGNAbout this report →
- Congenital Myasthenic SyndromeReads 1 of these genesPLECAbout this report →
- VitreoretinopathyReads 1 of these genesCOL11A1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesPLECAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesMBTPS2About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesMBTPS2About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesWASHC5About this report →
- Intellectual DisabilityReads 1 of these genesRPS6KA3About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesWASHC5About this report →
Vienu tyrimu sužinokite genus, susijusius su Small fingernail, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test40 genų susiję su Small fingernail
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Small fingernail. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| ERI1exoribonuclease 1 | Visada | 1 ligoje |
| FBXO28F-box protein 28 | Visada | 1 ligoje |
| FGFR2fibroblast growth factor receptor 2 | Visada | 1 ligoje |
| PIGOphosphatidylinositol glycan anchor biosynthesis class O | Visada | 1 ligoje |
| TBC1D24TBC1 domain family member 24 | Visada | 1 ligoje |
| HYMAIhydatidiform mole associated and imprinted | Labai dažnai (80–99%) | 1 ligoje |
| MSX1msh homeobox 1 | Labai dažnai (80–99%) | 1 ligoje |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Labai dažnai (80–99%) | 2 ligose |
| PLAGL1PLAG1 like zinc finger 1 | Labai dažnai (80–99%) | 1 ligoje |
| PLECplectin | Labai dažnai (80–99%) | 1 ligoje |
| SHOXSHOX homeobox | Labai dažnai (80–99%) | 1 ligoje |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Dažnai (30–79%) | 1 ligoje |
| CENPTcentromere protein T | Dažnai (30–79%) | 1 ligoje |
| COL11A1collagen type XI alpha 1 chain | Dažnai (30–79%) | 2 ligose |
| COL11A2collagen type XI alpha 2 chain | Dažnai (30–79%) | 1 ligoje |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Dažnai (30–79%) | 2 ligose |
| KCNN3potassium calcium-activated channel subfamily N member 3 | Dažnai (30–79%) | 1 ligoje |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Dažnai (30–79%) | 1 ligoje |
| PIGFphosphatidylinositol glycan anchor biosynthesis class F | Dažnai (30–79%) | 1 ligoje |
| RPS6KA3ribosomal protein S6 kinase A3 | Dažnai (30–79%) | 1 ligoje |
| ARHGAP31Rho GTPase activating protein 31 | Kartais (5–29%) | 1 ligoje |
| CCDC22CCC complex scaffolding subunit CCDC22 | Kartais (5–29%) | 1 ligoje |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Kartais (5–29%) | 1 ligoje |
| DLL4delta like canonical Notch ligand 4 | Kartais (5–29%) | 1 ligoje |
| DOCK6dedicator of cytokinesis 6 | Kartais (5–29%) | 1 ligoje |
| DPYSL5dihydropyrimidinase like 5 | Kartais (5–29%) | 1 ligoje |
| EOGTEGF domain specific O-linked N-acetylglucosamine transferase | Kartais (5–29%) | 1 ligoje |
| HMGA2high mobility group AT-hook 2 | Kartais (5–29%) | 1 ligoje |
| IGF2insulin like growth factor 2 | Kartais (5–29%) | 1 ligoje |
| NOTCH1notch receptor 1 | Kartais (5–29%) | 1 ligoje |
| PLAG1PLAG1 zinc finger | Kartais (5–29%) | 1 ligoje |
| PTDSS1phosphatidylserine synthase 1 | Kartais (5–29%) | 1 ligoje |
| RBPJrecombination signal binding protein for immunoglobulin kappa J region | Kartais (5–29%) | 1 ligoje |
| TWIST2twist family bHLH transcription factor 2 | Kartais (5–29%) | 1 ligoje |
| VPS35LVPS35 endosomal protein sorting factor like | Kartais (5–29%) | 1 ligoje |
| WASHC5WASH complex subunit 5 | Kartais (5–29%) | 1 ligoje |
| ZNF462zinc finger protein 462 | Retai (1–4 %) | 1 ligoje |
| BMPERBMP binding endothelial regulator | Neužfiksuota | 1 ligoje |
| ROR2ROR family WNT receptor 2 | Neužfiksuota | 1 ligoje |
| TFAP2Atranscription factor AP-2 alpha | Neužfiksuota | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
Siauresni požymiai
Platesni požymiai
Iš kur tai žinoma
- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.19-9814e911.
AtlasFrom 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.
Nemokamas pristatymas · Rezultatai per 6–8 savaites
