AtlasTræk
Absent fingernail
Absence of a fingernail.
Resumé
- Også kaldet
- Aplasia of the fingernail
- Kropssystem
- Abnormality of the integument
AtlasDenne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/absent-fingernail.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Absent fingernail, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test21 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 genesATP6V1B2TBC1D24About this report →
- Cenani-Lenz Syndactyly SyndromeReads 1 of these genesLRP4About this report →
- Focal Dermal Hypoplasia (Goltz Syndrome)Reads 1 of these genesPORCNAbout this report →
Show 17 more reports
- KCNH1-Related DisorderReads 1 of these genesKCNH1About this report →
- NOG-Related Symphalangism Spectrum DisorderReads 1 of these genesNOGAbout this report →
- Epidermolysis BullosaReads 3 of these genesDSPJUPCOL7A1About this report →
- Arrhythmogenic CardiomyopathyReads 2 of these genesDSPJUPAbout this report →
- Multiple Synostoses Syndrome (FGF9)Reads 1 of these genesNOGAbout this report →
- Colorectal Cancer & PolyposisReads 1 of these genesAPCAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesNOTCH1About this report →
- Noonan SyndromeReads 1 of these genesMAPK1About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesLRP4About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesFIG4About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesDSPAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesATP6V1B2TBC1D24About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesMAPK1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesFIG4About this report →
- Hearing Loss and DeafnessReads 1 of these genesTBC1D24About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesFIG4About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesFIG4About this report →
Læs de gener, der er knyttet til Absent fingernail, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test21 gener knyttet til Absent fingernail
Ændringer i disse gener forårsager sjældne tilstande, hvor Absent fingernail ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| DSPdesmoplakin | Altid | I 2 tilstande |
| APCAPC regulator of Wnt signaling pathway | Meget ofte (80–99 %) | I 1 tilstand |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Meget ofte (80–99 %) | I 3 tilstande |
| LRP4LDL receptor related protein 4 | Meget ofte (80–99 %) | I 1 tilstand |
| NOGnoggin | Meget ofte (80–99 %) | I 1 tilstand |
| TBC1D24TBC1 domain family member 24 | Meget ofte (80–99 %) | I 1 tilstand |
| BCRBCR activator of RhoGEF and GTPase | Ofte (30–79 %) | I 1 tilstand |
| CRKLCRK like proto-oncogene, adaptor protein | Ofte (30–79 %) | I 1 tilstand |
| FIG4FIG4 phosphoinositide 5-phosphatase | Ofte (30–79 %) | I 1 tilstand |
| JUPjunction plakoglobin | Ofte (30–79 %) | I 1 tilstand |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Ofte (30–79 %) | I 1 tilstand |
| KCNN3potassium calcium-activated channel subfamily N member 3 | Ofte (30–79 %) | I 1 tilstand |
| MAPK1mitogen-activated protein kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| ARHGAP31Rho GTPase activating protein 31 | Nogle gange (5–29 %) | I 1 tilstand |
| COL7A1collagen type VII alpha 1 chain | Nogle gange (5–29 %) | I 1 tilstand |
| DLL4delta like canonical Notch ligand 4 | Nogle gange (5–29 %) | I 1 tilstand |
| DOCK6dedicator of cytokinesis 6 | Nogle gange (5–29 %) | I 1 tilstand |
| EOGTEGF domain specific O-linked N-acetylglucosamine transferase | Nogle gange (5–29 %) | I 1 tilstand |
| NOTCH1notch receptor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RBPJrecombination signal binding protein for immunoglobulin kappa J region | Nogle gange (5–29 %) | I 1 tilstand |
| PORCNporcupine O-acyltransferase | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Snævrere træk
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
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Gratis forsendelse · Resultater på 6–8 uger
