AtlasPožymis
Absent nails
Klinikinis pavadinimas: Anonychia
Aplasia of the nail.
Santrauka
- Taip pat vadinama
- Aplastic nails
- 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/anonychia.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Absent nails, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
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.
- Epidermolysis BullosaReads 9 of these genesDSPCOL17A1COL7A1ITGB4LAMA3LAMB3About this report →
- Ectodermal DysplasiasReads 3 of these genesGJB6TP63WNT10AAbout this report →
- Darier and Hailey-Hailey DiseaseReads 1 of these genesATP2A2About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 4 of these genesDSPGJB6GRHL2WNT10AAbout this report →
Show 14 more reports
- Hereditary Corneal DystrophiesReads 2 of these genesCOL17A1GRHL2About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesACTG2About this report →
- Congenital Myasthenic SyndromeReads 2 of these genesLRP4PLECAbout this report →
- Hypodontia and AnodontiaReads 1 of these genesWNT10AAbout this report →
- Hearing Loss and DeafnessReads 3 of these genesGJB6GRHL2TBC1D24About this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesDSPAbout this report →
- Amelogenesis ImperfectaReads 1 of these genesLAMB3About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesFIG4About this report →
- Diabetes MellitusReads 1 of these genesZBTB20About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesPLECAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesATP6V1B2TBC1D24About this report →
- Female InfertilityReads 1 of these genesTP63About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesFIG4About this report →
- Intellectual DisabilityReads 1 of these genesARID1BAbout this report →
Vienu tyrimu sužinokite genus, susijusius su Absent nails, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test33 genų susiję su Absent nails
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Absent nails. 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 |
|---|---|---|
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Visada | 1 ligoje |
| DSPdesmoplakin | Visada | 1 ligoje |
| HOXA13homeobox A13 | Visada | 1 ligoje |
| RBBP8RB binding protein 8, endonuclease | Visada | 1 ligoje |
| RSPO4R-spondin 4 | Visada | 1 ligoje |
| LRP4LDL receptor related protein 4 | Labai dažnai (80–99%) | 1 ligoje |
| COL17A1collagen type XVII alpha 1 chain | Dažnai (30–79%) | 2 ligose |
| COL7A1collagen type VII alpha 1 chain | Dažnai (30–79%) | 5 ligose |
| FIG4FIG4 phosphoinositide 5-phosphatase | Dažnai (30–79%) | 1 ligoje |
| ITGB4integrin subunit beta 4 | Dažnai (30–79%) | 2 ligose |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Dažnai (30–79%) | 1 ligoje |
| LAMA3laminin subunit alpha 3 | Dažnai (30–79%) | 2 ligose |
| LAMB3laminin subunit beta 3 | Dažnai (30–79%) | 2 ligose |
| LAMC2laminin subunit gamma 2 | Dažnai (30–79%) | 2 ligose |
| MMP1matrix metallopeptidase 1 | Dažnai (30–79%) | 1 ligoje |
| ZBTB20zinc finger and BTB domain containing 20 | Dažnai (30–79%) | 1 ligoje |
| ACTG2actin gamma 2, smooth muscle | Kartais (5–29%) | 1 ligoje |
| ATP2A2ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 | Kartais (5–29%) | 1 ligoje |
| GJB6gap junction protein beta 6 | Kartais (5–29%) | 1 ligoje |
| PORCNporcupine O-acyltransferase | Kartais (5–29%) | 1 ligoje |
| SLC25A24solute carrier family 25 member 24 | Retai (1–4 %) | 1 ligoje |
| ARID1BAT-rich interaction domain 1B | Neužfiksuota | 1 ligoje |
| GRHL2grainyhead like transcription factor 2 | Neužfiksuota | 1 ligoje |
| ITGA6integrin subunit alpha 6 | Neužfiksuota | 1 ligoje |
| LMX1BLIM homeobox transcription factor 1 beta | Neužfiksuota | 1 ligoje |
| NOGnoggin | Neužfiksuota | 1 ligoje |
| PLECplectin | Neužfiksuota | 1 ligoje |
| RIPK4receptor interacting serine/threonine kinase 4 | Neužfiksuota | 1 ligoje |
| ROR2ROR family WNT receptor 2 | Neužfiksuota | 1 ligoje |
| TBC1D24TBC1 domain family member 24 | Neužfiksuota | 1 ligoje |
| TP63tumor protein p63 | Neužfiksuota | 1 ligoje |
| WNT10AWnt family member 10A | Neužfiksuota | 1 ligoje |
| WNT7AWnt family member 7A | Neužfiksuota | 2 ligose |
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 2026.10.17-8666dff2.
AtlasFrom traits to your genome
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