PRIMPOL gene related symptoms and diseases
All the information presented here about the PRIMPOL gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to PRIMPOL gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Cataract | Very Common - Between 80% and 100% cases |
| Myopia | Very Common - Between 80% and 100% cases |
| Visual loss | Very Common - Between 80% and 100% cases |
| Reduced visual acuity | Very Common - Between 80% and 100% cases |
| High myopia | Very Common - Between 80% and 100% cases |
Rare diseases associated to PRIMPOL gene
Here you will find a list of rare diseases related to the PRIMPOL. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
MYOPIA 22, AUTOSOMAL DOMINANT; MYP22
Description
Myopia, or nearsightedness, is a refractive error of the eye. Light rays from a distant object are focused in front of the retina and those from a near object are focused in the retina; therefore distant objects are blurry and near objects are clear (summary by Kaiser et al., 2004).For a discussion of genetic heterogeneity of susceptibility to myopia, see {160700}.
Most common symptoms of MYOPIA 22, AUTOSOMAL DOMINANT; MYP22
- Cataract
- Myopia
- Visual loss
- Reduced visual acuity
- High myopia
More info about MYOPIA 22, AUTOSOMAL DOMINANT; MYP22
SOURCES: OMIM
Search interest in PRIMPOL
Potential gene panels for PRIMPOL gene
PRIMPOL Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the PRIMPOL gene.
More info about this panel United States.
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