AtlasPožymis
Patchy baldness
Klinikinis pavadinimas: Patchy alopecia
Transient, non-scarring hair loss and preservation of the hair follicle located in in well-defined patches.
Santrauka
- Taip pat vadinama
- Alopecia areata
- Kūno sistema
- Abnormality of the integument
AtlasŠi puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/patchy-alopecia.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Patchy baldness, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test25 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.
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 6 of these genesDSG4HRKRT81KRT83KRT86PADI3About this report →
- Autoimmune Polyendocrine Syndrome Type 1 (APECED)Reads 1 of these genesAIREAbout this report →
- Lipoid ProteinosisReads 1 of these genesECM1About this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
Show 21 more report
- Ectodermal DysplasiasReads 2 of these genesNECTIN4TP63About this report →
- Epidermolysis BullosaReads 2 of these genesCOL17A1LAMB3About this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesADAM17About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesIL2RAAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Urea Cycle DisorderReads 1 of these genesASLAbout this report →
- Amelogenesis ImperfectaReads 1 of these genesLAMB3About this report →
- Hereditary Corneal DystrophiesReads 1 of these genesCOL17A1About this report →
- Neonatal Diabetes MellitusReads 1 of these genesIL2RAAbout this report →
- Autoimmune DiseaseReads 1 of these genesAIREAbout this report →
- Noonan SyndromeReads 1 of these genesHRASAbout this report →
- Diabetes MellitusReads 1 of these genesIL2RAAbout this report →
- Thyroid CancerReads 1 of these genesAIREAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Female InfertilityReads 1 of these genesTP63About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesHRASAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Epilepsy (Full Panel)Reads 1 of these genesKDM5CAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesIL2RAAbout this report →
- Intellectual DisabilityReads 1 of these genesKDM5CAbout this report →
Vienu tyrimu sužinokite genus, susijusius su Patchy baldness, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test28 genų susiję su Patchy baldness
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Patchy baldness. 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 |
|---|---|---|
| COL17A1collagen type XVII alpha 1 chain | Visada | 1 ligoje |
| IL2RAinterleukin 2 receptor subunit alpha | Visada | 1 ligoje |
| LAMB3laminin subunit beta 3 | Visada | 1 ligoje |
| TRA2Btransformer 2 beta homolog | Visada | 1 ligoje |
| DSG4desmoglein 4 | Labai dažnai (80–99%) | 1 ligoje |
| EBPEBP cholestenol delta-isomerase | Labai dažnai (80–99%) | 2 ligose |
| HRHR lysine demethylase and nuclear receptor corepressor | Labai dažnai (80–99%) | 1 ligoje |
| KDM5Clysine demethylase 5C | Labai dažnai (80–99%) | 2 ligose |
| KRT81keratin 81 | Labai dažnai (80–99%) | 1 ligoje |
| KRT83keratin 83 | Labai dažnai (80–99%) | 1 ligoje |
| KRT86keratin 86 | Labai dažnai (80–99%) | 1 ligoje |
| EXOSC2exosome component 2 | Dažnai (30–79%) | 1 ligoje |
| LMNAlamin A/C | Dažnai (30–79%) | 1 ligoje |
| PORCNporcupine O-acyltransferase | Dažnai (30–79%) | 2 ligose |
| TRACT cell receptor alpha constant | Dažnai (30–79%) | 1 ligoje |
| ZMPSTE24zinc metallopeptidase STE24 | Dažnai (30–79%) | 1 ligoje |
| AIREautoimmune regulator | Kartais (5–29%) | 1 ligoje |
| ASLargininosuccinate lyase | Kartais (5–29%) | 1 ligoje |
| BLMBLM RecQ like helicase | Kartais (5–29%) | 1 ligoje |
| KCTD1potassium channel tetramerization domain containing 1 | Kartais (5–29%) | 1 ligoje |
| PADI3peptidyl arginine deiminase 3 | Kartais (5–29%) | 1 ligoje |
| SEL1LSEL1L adaptor subunit of SYVN1 ubiquitin ligase | Kartais (5–29%) | 1 ligoje |
| TGM3transglutaminase 3 | Kartais (5–29%) | 1 ligoje |
| HRASHRas proto-oncogene, GTPase | Retai (1–4 %) | 1 ligoje |
| ADAM17ADAM metallopeptidase domain 17 | Neužfiksuota | 1 ligoje |
| ECM1extracellular matrix protein 1 | Neužfiksuota | 1 ligoje |
| NECTIN4nectin cell adhesion molecule 4 | Neužfiksuota | 1 ligoje |
| TP63tumor protein p63 | 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.
Siauresni požymiai
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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 2026.10.17-8666dff2.
AtlasFrom 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 470+ physician-ready reports.
Nemokamas pristatymas · Rezultatai per 6–8 savaites
