OPN1SW gene related symptoms and diseases
All the information presented here about the OPN1SW gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,OMIM,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to OPN1SW gene
Symptoms // Phenotype | % Cases |
---|---|
Optic atrophy | Very Common - Between 80% and 100% cases |
Confusion | Very Common - Between 80% and 100% cases |
Dyschromatopsia | Very Common - Between 80% and 100% cases |
Tritanomaly | Very Common - Between 80% and 100% cases |
Abnormal light-adapted electroretinogram | Very Common - Between 80% and 100% cases |
Rare diseases associated to OPN1SW gene
Here you will find a list of rare diseases related to the OPN1SW. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
TRITANOPIA
Alternate names
TRITANOPIA Is also known as blue colorblindness, tritan colour blindness, blue colour blindness, colorblindness, tritanopic, congenital tritanopia, colorblindness, tritan, cbt
Description
Tritanopia is an extremely rare form of colour blindness characterised by a selective deficiency of blue vision.
Most common symptoms of TRITANOPIA
- Optic atrophy
- Confusion
- Dyschromatopsia
- Tritanomaly
- Abnormal light-adapted electroretinogram
More info about TRITANOPIA
Search interest in OPN1SW
Potential gene panels for OPN1SW gene
OPN1SW Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the OPN1SW 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 ACTA2 TSPEAR COL1A2 BMS1 SMCHD1 BTLA ASPA