Egenskap
Moderate visual impairment
Kliniskt namn: Moderately reduced visual acuity
Moderate reduction of the ability to see. On the 6m visual acuity scale, moderate reduction is defined as less than 6/18 but at least 6/60. On the 20ft visual acuity scale, moderate reduction is defined as less than 20/70 but at least 20/200. On the decimal visual acuity scale, moderate reduction is defined as less than 0.3 but at least 0.1.
Sammanfattning
- Även kallad
- Moderate reduction in visual acuity, Moderate vision loss, Moderate visual loss
- Kroppssystem
- Abnormality of the eye
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library(jsonlite)
url <- "https://dantelabs.com/traits/moderately-reduced-visual-acuity.json"
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page$trait$nameLäs generna kopplade till Moderate visual impairment, och resten av ditt genom, med ett enda test.
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Beställ mitt Genome Test27 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.
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Läs generna kopplade till Moderate visual impairment, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test15 gener kopplade till Moderate visual impairment
Förändringar i dessa gener orsakar sällsynta tillstånd där Moderate visual impairment förekommer. De flesta med denna egenskap har inget av dessa tillstånd, och en gen på listan säger ingenting om någons eget genom.
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| CFAP20cilia and flagella associated protein 20 | Alltid | I 1 tillstånd |
| CNGB3cyclic nucleotide gated channel subunit beta 3 | Alltid | I 1 tillstånd |
| FDXRferredoxin reductase | Alltid | I 1 tillstånd |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Alltid | I 1 tillstånd |
| RPGRIP1RPGR interacting protein 1 | Alltid | I 2 tillstånd |
| TMEM216transmembrane protein 216 | Alltid | I 1 tillstånd |
| AHRaryl hydrocarbon receptor | Ofta (30–79 %) | I 1 tillstånd |
| DNM1Ldynamin 1L | Ofta (30–79 %) | I 1 tillstånd |
| IMPG1interphotoreceptor matrix proteoglycan 1 | Ofta (30–79 %) | I 1 tillstånd |
| IMPG2interphotoreceptor matrix proteoglycan 2 | Ofta (30–79 %) | I 1 tillstånd |
| OPA1OPA1 mitochondrial dynamin like GTPase | Ofta (30–79 %) | I 1 tillstånd |
| PPIBpeptidylprolyl isomerase B | Ofta (30–79 %) | I 1 tillstånd |
| OTX2orthodenticle homeobox 2 | Ibland (5–29 %) | I 1 tillstånd |
| RAC1Rac family small GTPase 1 | Ibland (5–29 %) | I 1 tillstånd |
| LRP5LDL receptor related protein 5 | Sällan (1–4%) | I 1 tillstånd |
Hur ofta det förekommer hos personer med ett av genens tillstånd, den vanligaste frekvensen bland dem, enligt Human Phenotype Ontology. Dessa sidor beskriver egenskaper och forskningen bakom dem. De är inte en diagnos, och det är läkare eller genetisk rådgivare du bör fråga om symtom.
Bredare egenskaper
Varifrån informationen kommer
- Human Phenotype Ontology, version 2026-09-01: egenskapen, dess namn, definition och de gener som är kopplade till den. Läs mer på hpo.jax.org.
- Dataversion 2026.10.21-311f020e.
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