Požymis
Eyelids stay open
Klinikinis pavadinimas: Lagophthalmos
A condition in which the eyelids do not close to cover the eye completely.
Santrauka
- Taip pat vadinama
- Inability to close the eyelids
- Kūno sistema
- Abnormality of head or neck
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/lagophthalmos.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Eyelids stay open, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test17 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.
- Inherited IchthyosesReads 9 of these genesABCA12ALOX12BALOXE3CYP4F22LIPNNIPAL4About this report →
- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
- Au-Kline SyndromeReads 1 of these genesHNRNPKAbout this report →
- Blepharocheilodontic Syndrome 2 (CTNND1)Reads 1 of these genesCTNND1About this report →
Show 13 more reports
- NGLY1 DeficiencyReads 1 of these genesNGLY1About this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- Carey-Fineman-Ziter SyndromeReads 1 of these genesMYMKAbout this report →
- Hereditary Diffuse Gastric CancerReads 1 of these genesCDH1About this report →
- PRR12-Related Neuroocular SyndromeReads 1 of these genesPRR12About this report →
- EBV-Driven Lymphoproliferation and CARD11 Immune DysregulationReads 1 of these genesIKZF2About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 1 of these genesCDH1About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesPOLR3AAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesIKZF2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesIKZF2About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesPOLR3AAbout this report →
Vienu tyrimu sužinokite genus, susijusius su Eyelids stay open, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test23 genų susiję su Eyelids stay open
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Eyelids stay open. 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 |
|---|---|---|
| CDH1cadherin 1 | Visada | 1 ligoje |
| DLX4distal-less homeobox 4 | Visada | 1 ligoje |
| HOXB1homeobox B1 | Visada | 1 ligoje |
| IKZF2IKAROS family zinc finger 2 | Visada | 1 ligoje |
| MYMKmyomaker, myoblast fusion factor | Visada | 1 ligoje |
| ABCA12ATP binding cassette subfamily A member 12 | Dažnai (30–79%) | 1 ligoje |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Dažnai (30–79%) | 1 ligoje |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Dažnai (30–79%) | 1 ligoje |
| ASPRV1aspartic peptidase retroviral like 1 | Dažnai (30–79%) | 1 ligoje |
| CTNND1catenin delta 1 | Dažnai (30–79%) | 1 ligoje |
| CYP4F22cytochrome P450 family 4 subfamily F member 22 | Dažnai (30–79%) | 1 ligoje |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Dažnai (30–79%) | 1 ligoje |
| LIPNlipase family member N | Dažnai (30–79%) | 1 ligoje |
| NIPAL4NIPA like domain containing 4 | Dažnai (30–79%) | 1 ligoje |
| PRR12proline rich 12 | Dažnai (30–79%) | 1 ligoje |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Dažnai (30–79%) | 1 ligoje |
| SULT2B1sulfotransferase family 2B member 1 | Dažnai (30–79%) | 1 ligoje |
| TGM1transglutaminase 1 | Dažnai (30–79%) | 1 ligoje |
| ECEL1endothelin converting enzyme like 1 | Kartais (5–29%) | 1 ligoje |
| KDM6Alysine demethylase 6A | Kartais (5–29%) | 1 ligoje |
| KMT2Dlysine methyltransferase 2D | Kartais (5–29%) | 1 ligoje |
| NGLY1N-glycanase 1 | Retai (1–4 %) | 1 ligoje |
| POLR3ARNA polymerase III subunit A | Retai (1–4 %) | 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 2026.10.19-9814e911.
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