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Özellik
Abnormality of the nail
Klinik adı: Abnormal nail morphology
Abnormal structure or appearance of the nail.
Özet
- Diğer adları
- Nail disease
- Vücut sistemi
- Abnormality of the integument
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Bu sayfanın veri olarak görünümü
Veriyi JSON olarak okumak için sayfa adresinin sonuna .json ekleyin veya application/json isteyin.
library(jsonlite)
url <- "https://dantelabs.com/traits/abnormal-nail-morphology.json"
page <- fromJSON(url)
page$trait$nameAbnormality of the nailHP:0001597
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Abnormality of the nail ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi al63 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 →
Abnormality of the nail ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi alAbnormality of the nail ile ilişkili 85 gen
Bu genlerdeki değişiklikler, Abnormality of the nail özelliğinin görüldüğü nadir durumlara yol açar. Bu özelliğe sahip çoğu kişide bu durumlardan hiçbiri yoktur; ayrıca bu listedeki bir gen, kimsenin kendi genomu hakkında bir şey söylemez.
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| LAMC2laminin subunit gamma 2 | Her zaman | 2 durumda |
| ACANaggrecan | Çok sık (%80–99) | 1 durumda |
| AP1S3adaptor related protein complex 1 subunit sigma 3 | Çok sık (%80–99) | 1 durumda |
| ATP2A2ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 | Çok sık (%80–99) | 1 durumda |
| CLEC7AC-type lectin domain containing 7A | Çok sık (%80–99) | 1 durumda |
| DSG4desmoglein 4 | Çok sık (%80–99) | 1 durumda |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Çok sık (%80–99) | 1 durumda |
| EVCEvC ciliary complex subunit 1 | Çok sık (%80–99) | 1 durumda |
| EVC2EvC ciliary complex subunit 2 | Çok sık (%80–99) | 1 durumda |
| GJA1gap junction protein alpha 1 | Çok sık (%80–99) | 3 durumda |
| GLI1GLI family zinc finger 1 | Çok sık (%80–99) | 1 durumda |
| HLA-Bmajor histocompatibility complex, class I, B | Çok sık (%80–99) | 1 durumda |
| IL17Finterleukin 17F | Çok sık (%80–99) | 1 durumda |
| IL17RAinterleukin 17 receptor A | Çok sık (%80–99) | 1 durumda |
| IL17RCinterleukin 17 receptor C | Çok sık (%80–99) | 1 durumda |
| IL36RNinterleukin 36 receptor antagonist | Çok sık (%80–99) | 1 durumda |
| KRT81keratin 81 | Çok sık (%80–99) | 1 durumda |
| KRT83keratin 83 | Çok sık (%80–99) | 1 durumda |
| KRT86keratin 86 | Çok sık (%80–99) | 1 durumda |
| LAMA3laminin subunit alpha 3 | Çok sık (%80–99) | 1 durumda |
| LAMB3laminin subunit beta 3 | Çok sık (%80–99) | 1 durumda |
| LMX1BLIM homeobox transcription factor 1 beta | Çok sık (%80–99) | 1 durumda |
| MSX1msh homeobox 1 | Çok sık (%80–99) | 1 durumda |
| PDE4Dphosphodiesterase 4D | Çok sık (%80–99) | 1 durumda |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Çok sık (%80–99) | 1 durumda |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Çok sık (%80–99) | 1 durumda |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Çok sık (%80–99) | 1 durumda |
| SLC25A24solute carrier family 25 member 24 | Çok sık (%80–99) | 1 durumda |
| SMARCAD1SNF2 related chromatin remodeling ATPase with DExD box 1 | Çok sık (%80–99) | 1 durumda |
| TP63tumor protein p63 | Çok sık (%80–99) | 1 durumda |
| TRAF3IP2TRAF3 interacting protein 2 | Çok sık (%80–99) | 1 durumda |
| ABCA12ATP binding cassette subfamily A member 12 | Sık (%30–79) | 1 durumda |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Sık (%30–79) | 1 durumda |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Sık (%30–79) | 1 durumda |
| CARD14caspase recruitment domain family member 14 | Sık (%30–79) | 1 durumda |
| CASRcalcium sensing receptor | Sık (%30–79) | 1 durumda |
| CERS3ceramide synthase 3 | Sık (%30–79) | 1 durumda |
| CTSCcathepsin C | Sık (%30–79) | 1 durumda |
| CTSKcathepsin K | Sık (%30–79) | 1 durumda |
| CYB5Acytochrome b5 type A | Sık (%30–79) | 1 durumda |
45 gen daha göster
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| CYB5R3cytochrome b5 reductase 3 | Sık (%30–79) | 1 durumda |
| DLX3distal-less homeobox 3 | Sık (%30–79) | 1 durumda |
| DSG1desmoglein 1 | Sık (%30–79) | 1 durumda |
| DSPdesmoplakin | Sık (%30–79) | 1 durumda |
| GNA11G protein subunit alpha 11 | Sık (%30–79) | 1 durumda |
| HGDhomogentisate 1,2-dioxygenase | Sık (%30–79) | 1 durumda |
| IFT140intraflagellar transport 140 | Sık (%30–79) | 1 durumda |
| IRF6interferon regulatory factor 6 | Sık (%30–79) | 1 durumda |
| KRT1keratin 1 | Sık (%30–79) | 1 durumda |
| LMNAlamin A/C | Sık (%30–79) | 2 durumda |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Sık (%30–79) | 1 durumda |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Sık (%30–79) | 1 durumda |
| NIPAL4NIPA like domain containing 4 | Sık (%30–79) | 1 durumda |
| PNPLA1patatin like domain 1, omega-hydroxyceramide transacylase | Sık (%30–79) | 1 durumda |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Sık (%30–79) | 1 durumda |
| SLC39A4solute carrier family 39 member 4 | Sık (%30–79) | 1 durumda |
| SULT2B1sulfotransferase family 2B member 1 | Sık (%30–79) | 1 durumda |
| TGM1transglutaminase 1 | Sık (%30–79) | 1 durumda |
| ADNPactivity dependent neuroprotector homeobox | Bazen (%5–29) | 1 durumda |
| AKT1AKT serine/threonine kinase 1 | Bazen (%5–29) | 1 durumda |
| CD28CD28 molecule | Bazen (%5–29) | 1 durumda |
| COX7Bcytochrome c oxidase subunit 7B | Bazen (%5–29) | 1 durumda |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Bazen (%5–29) | 1 durumda |
| EBPEBP cholestenol delta-isomerase | Bazen (%5–29) | 1 durumda |
| FBXO22F-box protein 22 | Bazen (%5–29) | 1 durumda |
| FGF9fibroblast growth factor 9 | Bazen (%5–29) | 1 durumda |
| FGFR2fibroblast growth factor receptor 2 | Bazen (%5–29) | 1 durumda |
| FUCA1alpha-L-fucosidase 1 | Bazen (%5–29) | 1 durumda |
| GDF5growth differentiation factor 5 | Bazen (%5–29) | 1 durumda |
| GDF6growth differentiation factor 6 | Bazen (%5–29) | 1 durumda |
| GJB2gap junction protein beta 2 | Bazen (%5–29) | 1 durumda |
| GJB3gap junction protein beta 3 | Bazen (%5–29) | 1 durumda |
| GJB4gap junction protein beta 4 | Bazen (%5–29) | 1 durumda |
| HCCSholocytochrome c synthase | Bazen (%5–29) | 1 durumda |
| HRHR lysine demethylase and nuclear receptor corepressor | Bazen (%5–29) | 1 durumda |
| KDSR3-ketodihydrosphingosine reductase | Bazen (%5–29) | 1 durumda |
| LEF1lymphoid enhancer binding factor 1 | Bazen (%5–29) | 1 durumda |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Bazen (%5–29) | 1 durumda |
| NOGnoggin | Bazen (%5–29) | 1 durumda |
| TATtyrosine aminotransferase | Bazen (%5–29) | 1 durumda |
| TNFRSF1BTNF receptor superfamily member 1B | Bazen (%5–29) | 1 durumda |
| TREX1three prime repair exonuclease 1 | Bazen (%5–29) | 1 durumda |
| CDSNcorneodesmosin | Kaydedilmedi | 1 durumda |
| KRT74keratin 74 | Kaydedilmedi | 1 durumda |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Kaydedilmedi | 1 durumda |
Bu özelliğin, genin ilişkili olduğu durumlardan birine sahip kişiler arasında ne sıklıkta görüldüğü; Human Phenotype Ontology'nin kaydettiği şekliyle, bunlar arasında en sık görülen oran. Bu sayfalar özellikleri ve bunların arkasındaki araştırmaları anlatır; tanı koymaz. Belirtiler hakkında bir doktora veya genetik danışmana başvurmanız gerekir.
Daha dar özellikler
- Poor nail formation130 gen
- Abnormal fingernails99 gen
- Atypical nail growth84 gen
- Brittle nails35 gen
- Abnormality of the toenail33 gen
- Thick nail19 gen
- Absent/small nails16 gen
- Thin nail16 gen
- Abnormal periungual morphology3 gen
- Abnormality of nail color3 gen
- Nailfold capillary tortuosity3 gen
- Chronic monilial nail infection2 gen
- Nail bed hemorrhage2 gen
- Nail bed telangiectasia2 gen
- Abnormal subungual morphology1 gen
- Longitudinal erythronychia1 gen
- Onychoheterotopia1 gen
- Pyramidal skinfold extending from the base to the top of the nails1 gen
- Splinter hemorrhages1 gen
- Abnormal nail attachment
- Abnormal nail growth
- Abnormal nail surface
- Nail tumor
Daha geniş özellikler
Bilgilerin kaynağı
- Human Phenotype Ontology, 2026-09-01 sürümü: özellik, adları, tanımı ve buna bağlı genler. Ayrıntılar için hpo.jax.org adresine bakın.
- Veri sürümü 2026.10.19-9814e911.
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
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$449'den başlayan
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