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Egenskap
Abnormality of the nail
Klinisk navn: Abnormal nail morphology
Abnormal structure or appearance of the nail.
Sammendrag
- Også kalt
- Nail disease
- Kroppssystem
- Abnormality of the integument
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Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/abnormal-nail-morphology.json"
page <- fromJSON(url)
page$trait$nameAbnormality of the nailHP:0001597
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Les genene knyttet til Abnormality of the nail, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt 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 →
Les genene knyttet til Abnormality of the nail, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test85 gener knyttet til Abnormality of the nail
Endringer i disse genene forårsaker sjeldne tilstander der Abnormality of the nail forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| LAMC2laminin subunit gamma 2 | Alltid | I 2 tilstander |
| ACANaggrecan | Svært ofte (80–99 %) | I 1 tilstand |
| AP1S3adaptor related protein complex 1 subunit sigma 3 | Svært ofte (80–99 %) | I 1 tilstand |
| ATP2A2ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 | Svært ofte (80–99 %) | I 1 tilstand |
| CLEC7AC-type lectin domain containing 7A | Svært ofte (80–99 %) | I 1 tilstand |
| DSG4desmoglein 4 | Svært ofte (80–99 %) | I 1 tilstand |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Svært ofte (80–99 %) | I 1 tilstand |
| EVCEvC ciliary complex subunit 1 | Svært ofte (80–99 %) | I 1 tilstand |
| EVC2EvC ciliary complex subunit 2 | Svært ofte (80–99 %) | I 1 tilstand |
| GJA1gap junction protein alpha 1 | Svært ofte (80–99 %) | I 3 tilstander |
| GLI1GLI family zinc finger 1 | Svært ofte (80–99 %) | I 1 tilstand |
| HLA-Bmajor histocompatibility complex, class I, B | Svært ofte (80–99 %) | I 1 tilstand |
| IL17Finterleukin 17F | Svært ofte (80–99 %) | I 1 tilstand |
| IL17RAinterleukin 17 receptor A | Svært ofte (80–99 %) | I 1 tilstand |
| IL17RCinterleukin 17 receptor C | Svært ofte (80–99 %) | I 1 tilstand |
| IL36RNinterleukin 36 receptor antagonist | Svært ofte (80–99 %) | I 1 tilstand |
| KRT81keratin 81 | Svært ofte (80–99 %) | I 1 tilstand |
| KRT83keratin 83 | Svært ofte (80–99 %) | I 1 tilstand |
| KRT86keratin 86 | Svært ofte (80–99 %) | I 1 tilstand |
| LAMA3laminin subunit alpha 3 | Svært ofte (80–99 %) | I 1 tilstand |
| LAMB3laminin subunit beta 3 | Svært ofte (80–99 %) | I 1 tilstand |
| LMX1BLIM homeobox transcription factor 1 beta | Svært ofte (80–99 %) | I 1 tilstand |
| MSX1msh homeobox 1 | Svært ofte (80–99 %) | I 1 tilstand |
| PDE4Dphosphodiesterase 4D | Svært ofte (80–99 %) | I 1 tilstand |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Svært ofte (80–99 %) | I 1 tilstand |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Svært ofte (80–99 %) | I 1 tilstand |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Svært ofte (80–99 %) | I 1 tilstand |
| SLC25A24solute carrier family 25 member 24 | Svært ofte (80–99 %) | I 1 tilstand |
| SMARCAD1SNF2 related chromatin remodeling ATPase with DExD box 1 | Svært ofte (80–99 %) | I 1 tilstand |
| TP63tumor protein p63 | Svært ofte (80–99 %) | I 1 tilstand |
| TRAF3IP2TRAF3 interacting protein 2 | Svært ofte (80–99 %) | I 1 tilstand |
| ABCA12ATP binding cassette subfamily A member 12 | Ofte (30–79 %) | I 1 tilstand |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Ofte (30–79 %) | I 1 tilstand |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Ofte (30–79 %) | I 1 tilstand |
| CARD14caspase recruitment domain family member 14 | Ofte (30–79 %) | I 1 tilstand |
| CASRcalcium sensing receptor | Ofte (30–79 %) | I 1 tilstand |
| CERS3ceramide synthase 3 | Ofte (30–79 %) | I 1 tilstand |
| CTSCcathepsin C | Ofte (30–79 %) | I 1 tilstand |
| CTSKcathepsin K | Ofte (30–79 %) | I 1 tilstand |
| CYB5Acytochrome b5 type A | Ofte (30–79 %) | I 1 tilstand |
Vis 45 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| CYB5R3cytochrome b5 reductase 3 | Ofte (30–79 %) | I 1 tilstand |
| DLX3distal-less homeobox 3 | Ofte (30–79 %) | I 1 tilstand |
| DSG1desmoglein 1 | Ofte (30–79 %) | I 1 tilstand |
| DSPdesmoplakin | Ofte (30–79 %) | I 1 tilstand |
| GNA11G protein subunit alpha 11 | Ofte (30–79 %) | I 1 tilstand |
| HGDhomogentisate 1,2-dioxygenase | Ofte (30–79 %) | I 1 tilstand |
| IFT140intraflagellar transport 140 | Ofte (30–79 %) | I 1 tilstand |
| IRF6interferon regulatory factor 6 | Ofte (30–79 %) | I 1 tilstand |
| KRT1keratin 1 | Ofte (30–79 %) | I 1 tilstand |
| LMNAlamin A/C | Ofte (30–79 %) | I 2 tilstander |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Ofte (30–79 %) | I 1 tilstand |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Ofte (30–79 %) | I 1 tilstand |
| NIPAL4NIPA like domain containing 4 | Ofte (30–79 %) | I 1 tilstand |
| PNPLA1patatin like domain 1, omega-hydroxyceramide transacylase | Ofte (30–79 %) | I 1 tilstand |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Ofte (30–79 %) | I 1 tilstand |
| SLC39A4solute carrier family 39 member 4 | Ofte (30–79 %) | I 1 tilstand |
| SULT2B1sulfotransferase family 2B member 1 | Ofte (30–79 %) | I 1 tilstand |
| TGM1transglutaminase 1 | Ofte (30–79 %) | I 1 tilstand |
| ADNPactivity dependent neuroprotector homeobox | Noen ganger (5–29 %) | I 1 tilstand |
| AKT1AKT serine/threonine kinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| CD28CD28 molecule | Noen ganger (5–29 %) | I 1 tilstand |
| COX7Bcytochrome c oxidase subunit 7B | Noen ganger (5–29 %) | I 1 tilstand |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Noen ganger (5–29 %) | I 1 tilstand |
| EBPEBP cholestenol delta-isomerase | Noen ganger (5–29 %) | I 1 tilstand |
| FBXO22F-box protein 22 | Noen ganger (5–29 %) | I 1 tilstand |
| FGF9fibroblast growth factor 9 | Noen ganger (5–29 %) | I 1 tilstand |
| FGFR2fibroblast growth factor receptor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| FUCA1alpha-L-fucosidase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GDF5growth differentiation factor 5 | Noen ganger (5–29 %) | I 1 tilstand |
| GDF6growth differentiation factor 6 | Noen ganger (5–29 %) | I 1 tilstand |
| GJB2gap junction protein beta 2 | Noen ganger (5–29 %) | I 1 tilstand |
| GJB3gap junction protein beta 3 | Noen ganger (5–29 %) | I 1 tilstand |
| GJB4gap junction protein beta 4 | Noen ganger (5–29 %) | I 1 tilstand |
| HCCSholocytochrome c synthase | Noen ganger (5–29 %) | I 1 tilstand |
| HRHR lysine demethylase and nuclear receptor corepressor | Noen ganger (5–29 %) | I 1 tilstand |
| KDSR3-ketodihydrosphingosine reductase | Noen ganger (5–29 %) | I 1 tilstand |
| LEF1lymphoid enhancer binding factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Noen ganger (5–29 %) | I 1 tilstand |
| NOGnoggin | Noen ganger (5–29 %) | I 1 tilstand |
| TATtyrosine aminotransferase | Noen ganger (5–29 %) | I 1 tilstand |
| TNFRSF1BTNF receptor superfamily member 1B | Noen ganger (5–29 %) | I 1 tilstand |
| TREX1three prime repair exonuclease 1 | Noen ganger (5–29 %) | I 1 tilstand |
| CDSNcorneodesmosin | Ikke registrert | I 1 tilstand |
| KRT74keratin 74 | Ikke registrert | I 1 tilstand |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Smalere egenskaper
- Poor nail formation130 gener
- Abnormal fingernails99 gener
- Atypical nail growth84 gener
- Brittle nails35 gener
- Abnormality of the toenail33 gener
- Thick nail19 gener
- Absent/small nails16 gener
- Thin nail16 gener
- Abnormal periungual morphology3 gener
- Abnormality of nail color3 gener
- Nailfold capillary tortuosity3 gener
- Chronic monilial nail infection2 gener
- Nail bed hemorrhage2 gener
- Nail bed telangiectasia2 gener
- 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
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.19-9814e911.
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