P4HA2 gene related symptoms and diseases
All the information presented here about the P4HA2 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to P4HA2 gene
Symptoms // Phenotype | % Cases |
---|---|
Myopia | Very Common - Between 80% and 100% cases |
High myopia | Very Common - Between 80% and 100% cases |
Rare diseases associated to P4HA2 gene
Here you will find a list of rare diseases related to the P4HA2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
MYOPIA 25, AUTOSOMAL DOMINANT; MYP25
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 25, AUTOSOMAL DOMINANT; MYP25
- Myopia
- High myopia
More info about MYOPIA 25, AUTOSOMAL DOMINANT; MYP25
SOURCES: OMIM
Search interest in P4HA2
Potential gene panels for P4HA2 gene
P4HA2 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the P4HA2 gene.
More info about this panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like TBX6 CD28 SLC6A2 JPH2 CA5A KAT6B WDR1