AtlasChi aiutiamoLa nostra scienzaProdottiRisultati
AccediChiediSequenzia il tuo genoma↗
Tratto
Abnormality of the nail
Nome clinico: Abnormal nail morphology
Abnormal structure or appearance of the nail.
Riepilogo
- Detto anche
- Nail disease
- Sistema corporeo
- Abnormality of the integument
AtlasChi aiutiamoLa nostra scienzaProdottiRisultati
AccediChiediSequenzia il tuo genoma↗
Questa pagina come dati
Aggiunga .json all'indirizzo della pagina, oppure richieda application/json, per leggerla come JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/abnormal-nail-morphology.json"
page <- fromJSON(url)
page$trait$nameAbnormality of the nailHP:0001597
AtlasChi aiutiamoLa nostra scienzaProdottiRisultati
AccediChiediSequenzia il tuo genoma↗
Leggi i geni collegati a Abnormality of the nail e il resto del tuo genoma con un unico test.
A partire da 449 $Spedizione gratuita · Risultati in 6–8 settimane
Ottieni il mio 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 →
Leggi i geni collegati a Abnormality of the nail e il resto del tuo genoma con un unico test.
A partire da 449 $Spedizione gratuita · Risultati in 6–8 settimane
Ottieni il mio Genome Test85 geni collegati a Abnormality of the nail
Alterazioni in questi geni causano malattie rare in cui si osserva Abnormality of the nail. La maggior parte delle persone con questo tratto non presenta nessuna di tali condizioni, e un gene di questo elenco non dice nulla sul genoma di nessuno in particolare.
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| LAMC2laminin subunit gamma 2 | Sempre | In 2 condizioni |
| ACANaggrecan | Molto spesso (80–99%) | In 1 condizione |
| AP1S3adaptor related protein complex 1 subunit sigma 3 | Molto spesso (80–99%) | In 1 condizione |
| ATP2A2ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 | Molto spesso (80–99%) | In 1 condizione |
| CLEC7AC-type lectin domain containing 7A | Molto spesso (80–99%) | In 1 condizione |
| DSG4desmoglein 4 | Molto spesso (80–99%) | In 1 condizione |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Molto spesso (80–99%) | In 1 condizione |
| EVCEvC ciliary complex subunit 1 | Molto spesso (80–99%) | In 1 condizione |
| EVC2EvC ciliary complex subunit 2 | Molto spesso (80–99%) | In 1 condizione |
| GJA1gap junction protein alpha 1 | Molto spesso (80–99%) | In 3 condizioni |
| GLI1GLI family zinc finger 1 | Molto spesso (80–99%) | In 1 condizione |
| HLA-Bmajor histocompatibility complex, class I, B | Molto spesso (80–99%) | In 1 condizione |
| IL17Finterleukin 17F | Molto spesso (80–99%) | In 1 condizione |
| IL17RAinterleukin 17 receptor A | Molto spesso (80–99%) | In 1 condizione |
| IL17RCinterleukin 17 receptor C | Molto spesso (80–99%) | In 1 condizione |
| IL36RNinterleukin 36 receptor antagonist | Molto spesso (80–99%) | In 1 condizione |
| KRT81keratin 81 | Molto spesso (80–99%) | In 1 condizione |
| KRT83keratin 83 | Molto spesso (80–99%) | In 1 condizione |
| KRT86keratin 86 | Molto spesso (80–99%) | In 1 condizione |
| LAMA3laminin subunit alpha 3 | Molto spesso (80–99%) | In 1 condizione |
| LAMB3laminin subunit beta 3 | Molto spesso (80–99%) | In 1 condizione |
| LMX1BLIM homeobox transcription factor 1 beta | Molto spesso (80–99%) | In 1 condizione |
| MSX1msh homeobox 1 | Molto spesso (80–99%) | In 1 condizione |
| PDE4Dphosphodiesterase 4D | Molto spesso (80–99%) | In 1 condizione |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Molto spesso (80–99%) | In 1 condizione |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Molto spesso (80–99%) | In 1 condizione |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Molto spesso (80–99%) | In 1 condizione |
| SLC25A24solute carrier family 25 member 24 | Molto spesso (80–99%) | In 1 condizione |
| SMARCAD1SNF2 related chromatin remodeling ATPase with DExD box 1 | Molto spesso (80–99%) | In 1 condizione |
| TP63tumor protein p63 | Molto spesso (80–99%) | In 1 condizione |
| TRAF3IP2TRAF3 interacting protein 2 | Molto spesso (80–99%) | In 1 condizione |
| ABCA12ATP binding cassette subfamily A member 12 | Spesso (30–79%) | In 1 condizione |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Spesso (30–79%) | In 1 condizione |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Spesso (30–79%) | In 1 condizione |
| CARD14caspase recruitment domain family member 14 | Spesso (30–79%) | In 1 condizione |
| CASRcalcium sensing receptor | Spesso (30–79%) | In 1 condizione |
| CERS3ceramide synthase 3 | Spesso (30–79%) | In 1 condizione |
| CTSCcathepsin C | Spesso (30–79%) | In 1 condizione |
| CTSKcathepsin K | Spesso (30–79%) | In 1 condizione |
| CYB5Acytochrome b5 type A | Spesso (30–79%) | In 1 condizione |
Mostra altri 45 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| CYB5R3cytochrome b5 reductase 3 | Spesso (30–79%) | In 1 condizione |
| DLX3distal-less homeobox 3 | Spesso (30–79%) | In 1 condizione |
| DSG1desmoglein 1 | Spesso (30–79%) | In 1 condizione |
| DSPdesmoplakin | Spesso (30–79%) | In 1 condizione |
| GNA11G protein subunit alpha 11 | Spesso (30–79%) | In 1 condizione |
| HGDhomogentisate 1,2-dioxygenase | Spesso (30–79%) | In 1 condizione |
| IFT140intraflagellar transport 140 | Spesso (30–79%) | In 1 condizione |
| IRF6interferon regulatory factor 6 | Spesso (30–79%) | In 1 condizione |
| KRT1keratin 1 | Spesso (30–79%) | In 1 condizione |
| LMNAlamin A/C | Spesso (30–79%) | In 2 condizioni |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Spesso (30–79%) | In 1 condizione |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Spesso (30–79%) | In 1 condizione |
| NIPAL4NIPA like domain containing 4 | Spesso (30–79%) | In 1 condizione |
| PNPLA1patatin like domain 1, omega-hydroxyceramide transacylase | Spesso (30–79%) | In 1 condizione |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Spesso (30–79%) | In 1 condizione |
| SLC39A4solute carrier family 39 member 4 | Spesso (30–79%) | In 1 condizione |
| SULT2B1sulfotransferase family 2B member 1 | Spesso (30–79%) | In 1 condizione |
| TGM1transglutaminase 1 | Spesso (30–79%) | In 1 condizione |
| ADNPactivity dependent neuroprotector homeobox | A volte (5–29%) | In 1 condizione |
| AKT1AKT serine/threonine kinase 1 | A volte (5–29%) | In 1 condizione |
| CD28CD28 molecule | A volte (5–29%) | In 1 condizione |
| COX7Bcytochrome c oxidase subunit 7B | A volte (5–29%) | In 1 condizione |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | A volte (5–29%) | In 1 condizione |
| EBPEBP cholestenol delta-isomerase | A volte (5–29%) | In 1 condizione |
| FBXO22F-box protein 22 | A volte (5–29%) | In 1 condizione |
| FGF9fibroblast growth factor 9 | A volte (5–29%) | In 1 condizione |
| FGFR2fibroblast growth factor receptor 2 | A volte (5–29%) | In 1 condizione |
| FUCA1alpha-L-fucosidase 1 | A volte (5–29%) | In 1 condizione |
| GDF5growth differentiation factor 5 | A volte (5–29%) | In 1 condizione |
| GDF6growth differentiation factor 6 | A volte (5–29%) | In 1 condizione |
| GJB2gap junction protein beta 2 | A volte (5–29%) | In 1 condizione |
| GJB3gap junction protein beta 3 | A volte (5–29%) | In 1 condizione |
| GJB4gap junction protein beta 4 | A volte (5–29%) | In 1 condizione |
| HCCSholocytochrome c synthase | A volte (5–29%) | In 1 condizione |
| HRHR lysine demethylase and nuclear receptor corepressor | A volte (5–29%) | In 1 condizione |
| KDSR3-ketodihydrosphingosine reductase | A volte (5–29%) | In 1 condizione |
| LEF1lymphoid enhancer binding factor 1 | A volte (5–29%) | In 1 condizione |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | A volte (5–29%) | In 1 condizione |
| NOGnoggin | A volte (5–29%) | In 1 condizione |
| TATtyrosine aminotransferase | A volte (5–29%) | In 1 condizione |
| TNFRSF1BTNF receptor superfamily member 1B | A volte (5–29%) | In 1 condizione |
| TREX1three prime repair exonuclease 1 | A volte (5–29%) | In 1 condizione |
| CDSNcorneodesmosin | Non registrato | In 1 condizione |
| KRT74keratin 74 | Non registrato | In 1 condizione |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Non registrato | In 1 condizione |
Con quale frequenza questo tratto si presenta tra le persone con una delle condizioni legate al gene, nella misura più alta riscontrata tra queste, secondo quanto registrato dall'Human Phenotype Ontology. Queste pagine descrivono tratti e la ricerca che li riguarda; non costituiscono una diagnosi, e per i sintomi il medico o il consulente genetico è la persona a cui rivolgersi.
Tratti più specifici
- Poor nail formation130 geni
- Abnormal fingernails99 geni
- Atypical nail growth84 geni
- Brittle nails35 geni
- Abnormality of the toenail33 geni
- Thick nail19 geni
- Absent/small nails16 geni
- Thin nail16 geni
- Abnormal periungual morphology3 geni
- Abnormality of nail color3 geni
- Nailfold capillary tortuosity3 geni
- Chronic monilial nail infection2 geni
- Nail bed hemorrhage2 geni
- Nail bed telangiectasia2 geni
- Abnormal subungual morphology1 gene
- Longitudinal erythronychia1 gene
- Onychoheterotopia1 gene
- Pyramidal skinfold extending from the base to the top of the nails1 gene
- Splinter hemorrhages1 gene
- Abnormal nail attachment
- Abnormal nail growth
- Abnormal nail surface
- Nail tumor
Tratti più generali
Fonte dei dati
- Human Phenotype Ontology, versione 2026-09-01: il tratto, i suoi nomi, la sua definizione e i geni a esso collegati. Per saperne di più visiti hpo.jax.org.
- Versione dei dati 2026.10.19-9814e911.
AtlasChi aiutiamoLa nostra scienzaProdottiRisultati
AccediChiediSequenzia il tuo genoma↗
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.
A partire da 449 $
Spedizione gratuita · Risultati in 6–8 settimane
