AtlasTræk
Skin erosion
A discontinuity of the skin exhibiting incomplete loss of the epidermis, a lesion that is moist, circumscribed, and usually depressed.
Resumé
- 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/skin-erosion.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Skin erosion, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test35 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.
- Epidermolysis BullosaReads 9 of these genesDSPLAMA3LAMB3LAMC2COL7A1ITGB4About this report →
- PorphyriaReads 3 of these genesPPOXURODUROSAbout this report →
- Focal Dermal Hypoplasia (Goltz Syndrome)Reads 1 of these genesPORCNAbout this report →
- Lipoid ProteinosisReads 1 of these genesECM1About this report →
Show 31 more reports
- PLEC-Related Epidermolysis Bullosa and Muscular DystrophyReads 1 of these genesPLECAbout this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- Inherited IchthyosesReads 4 of these genesKRT1KRT10CSTATGM5About this report →
- Hepatic Porphyria DisordersReads 2 of these genesPPOXURODAbout this report →
- Darier and Hailey-Hailey DiseaseReads 1 of these genesATP2C1About this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- LipodystrophyReads 2 of these genesZMPSTE24LMNAAbout this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesRIPK4About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 3 of these genesDSPKRT1KRT14About this report →
- Achondrogenesis panelReads 1 of these genesCOL2A1About this report →
- Hereditary Gastrointestinal Stromal TumourReads 1 of these genesKITAbout this report →
- Hereditary Vascular MalformationsReads 1 of these genesEPHB4About this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 1 of these genesGNA11About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesLMNAPLECAbout this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesCOL2A1About this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesDSPAbout this report →
- Diamond-Blackfan AnemiaReads 1 of these genesGATA1About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesEPHB4About this report →
- Amelogenesis ImperfectaReads 1 of these genesLAMB3About this report →
- Ectodermal DysplasiasReads 1 of these genesKRT14About this report →
- Autoimmune DiseaseReads 1 of these genesATP2C1About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesPLECAbout this report →
- VitreoretinopathyReads 1 of these genesCOL2A1About this report →
- Thyroid CancerReads 1 of these genesGNA11About this report →
- Inherited ThrombocytopeniasReads 1 of these genesGATA1About this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Congenital Disorders of GlycosylationReads 1 of these genesKRT5About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesLMNAAbout this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesNAXEAbout this report →
Læs de gener, der er knyttet til Skin erosion, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test29 gener knyttet til Skin erosion
Ændringer i disse gener forårsager sjældne tilstande, hvor Skin erosion 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 1 tilstand |
| KRT1keratin 1 | Altid | I 1 tilstand |
| KRT10keratin 10 | Altid | I 1 tilstand |
| PPOXprotoporphyrinogen oxidase | Altid | I 2 tilstande |
| ZMPSTE24zinc metallopeptidase STE24 | Altid | I 2 tilstande |
| ARL6IP6ARF like GTPase 6 interacting protein 6 | Meget ofte (80–99 %) | I 1 tilstand |
| ATP2C1ATPase secretory pathway Ca2+ transporting 1 | Meget ofte (80–99 %) | I 1 tilstand |
| COL2A1collagen type II alpha 1 chain | Meget ofte (80–99 %) | I 1 tilstand |
| GNA11G protein subunit alpha 11 | Meget ofte (80–99 %) | I 1 tilstand |
| LAMA3laminin subunit alpha 3 | Meget ofte (80–99 %) | I 2 tilstande |
| LAMB3laminin subunit beta 3 | Meget ofte (80–99 %) | I 1 tilstand |
| LAMC2laminin subunit gamma 2 | Meget ofte (80–99 %) | I 1 tilstand |
| LMNAlamin A/C | Meget ofte (80–99 %) | I 1 tilstand |
| COL7A1collagen type VII alpha 1 chain | Ofte (30–79 %) | I 4 tilstande |
| EPHB4EPH receptor B4 | Ofte (30–79 %) | I 1 tilstand |
| GATA1GATA binding protein 1 | Ofte (30–79 %) | I 1 tilstand |
| ITGB4integrin subunit beta 4 | Ofte (30–79 %) | I 1 tilstand |
| KRT14keratin 14 | Ofte (30–79 %) | I 2 tilstande |
| KRT5keratin 5 | Ofte (30–79 %) | I 2 tilstande |
| PLECplectin | Ofte (30–79 %) | I 2 tilstande |
| PORCNporcupine O-acyltransferase | Ofte (30–79 %) | I 1 tilstand |
| URODuroporphyrinogen decarboxylase | Ofte (30–79 %) | I 1 tilstand |
| UROSuroporphyrinogen III synthase | Ofte (30–79 %) | I 1 tilstand |
| CSTAcystatin A | Nogle gange (5–29 %) | I 1 tilstand |
| ECM1extracellular matrix protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| KITKIT proto-oncogene, receptor tyrosine kinase | Nogle gange (5–29 %) | I 1 tilstand |
| TGM5transglutaminase 5 | Nogle gange (5–29 %) | I 1 tilstand |
| NAXENAD(P)HX epimerase | Ikke registreret | I 1 tilstand |
| RIPK4receptor interacting serine/threonine kinase 4 | 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.
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.
AtlasFrom traits to your genome
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Gratis forsendelse · Resultater på 6–8 uger
