Požymis
Epidermoid cyst
Nontender, round and firm, but slightly compressible, intradermal or subcutaneous cyst measuring 0.5-5 cm in diameter. Epidermal cysts are intradermal or subcutaneous tumors, grow slowly and occur on the face, neck, back and scrotum. They usually appear at or around puberty, and as a rule an affected individual has one solitary or a few cysts. A central, dark comedone opening (punctum) may be present.
Santrauka
- Taip pat vadinama
- Epidermal cyst, Epidermal inclusion cyst, Infundibular cyst, Keratin cyst
- Kūno sistema
- Abnormality of the integument
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Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/epidermoid-cyst.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Epidermoid cyst, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test18 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.
- Tuberous SclerosisReads 2 of these genesTSC1TSC2About this report →
- Birt-Hogg-Dubé SyndromeReads 1 of these genesFLCNAbout this report →
- Blepharocheilodontic Syndrome 2 (CTNND1)Reads 1 of these genesCTNND1About this report →
- GAPO SyndromeReads 1 of these genesANTXR1About this report →
Show 14 more reports
- Familial Hidradenitis SuppurativaReads 1 of these genesPSENENAbout this report →
- Hereditary Diffuse Gastric CancerReads 1 of these genesCDH1About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 4 of these genesKRT17KRT6BKRT16KRT6AAbout this report →
- Mosaic Variegated Aneuploidy SyndromeReads 1 of these genesCEP57About this report →
- Colorectal Cancer & PolyposisReads 1 of these genesAPCAbout this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 1 of these genesCDH1About this report →
- Kidney CancerReads 1 of these genesFLCNAbout this report →
- Congenital Disorders of GlycosylationReads 3 of these genesKRT5POFUT1POGLUT1About this report →
- Urinary and Renal System TumourReads 1 of these genesFLCNAbout this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 1 of these genesCDH3About this report →
- Epidermolysis BullosaReads 1 of these genesKRT5About this report →
- Neonatal Diabetes MellitusReads 1 of these genesMNX1About this report →
- Diabetes MellitusReads 1 of these genesMNX1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesPOGLUT1About this report →
Vienu tyrimu sužinokite genus, susijusius su Epidermoid cyst, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test20 genų susiję su Epidermoid cyst
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Epidermoid cyst. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| CDH3cadherin 3 | Visada | 1 ligoje |
| KRT17keratin 17 | Visada | 2 ligose |
| KRT6Bkeratin 6B | Visada | 2 ligose |
| APCAPC regulator of Wnt signaling pathway | Dažnai (30–79%) | 3 ligose |
| CEP57centrosomal protein 57 | Dažnai (30–79%) | 1 ligoje |
| KRT16keratin 16 | Dažnai (30–79%) | 1 ligoje |
| KRT6Akeratin 6A | Dažnai (30–79%) | 1 ligoje |
| CDH1cadherin 1 | Kartais (5–29%) | 1 ligoje |
| CTNND1catenin delta 1 | Kartais (5–29%) | 1 ligoje |
| FLCNfolliculin | Kartais (5–29%) | 1 ligoje |
| IFNGinterferon gamma | Kartais (5–29%) | 1 ligoje |
| MNX1motor neuron and pancreas homeobox 1 | Kartais (5–29%) | 1 ligoje |
| PRDM10PR/SET domain 10 | Kartais (5–29%) | 1 ligoje |
| TSC1TSC complex subunit 1 | Kartais (5–29%) | 1 ligoje |
| TSC2TSC complex subunit 2 | Kartais (5–29%) | 1 ligoje |
| KRT5keratin 5 | Retai (1–4 %) | 1 ligoje |
| POFUT1protein O-fucosyltransferase 1 | Retai (1–4 %) | 1 ligoje |
| POGLUT1protein O-glucosyltransferase 1 | Retai (1–4 %) | 1 ligoje |
| PSENENpresenilin enhancer, gamma-secretase subunit | Retai (1–4 %) | 1 ligoje |
| ANTXR1ANTXR cell adhesion molecule 1 | Neužfiksuota | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
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Iš kur tai žinoma
- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.21-777c9289.
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