CYGB gene related symptoms and diseases
All the information presented here about the CYGB gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,HGNC, Mendelian Rare Disease Search Engine.
Table of contents:
Top 5 symptoms and clinical features associated to CYGB gene
Symptoms // Phenotype | % Cases |
---|---|
Cataract | Very Common - Between 80% and 100% cases |
Edema | Very Common - Between 80% and 100% cases |
Rod-cone dystrophy | Very Common - Between 80% and 100% cases |
Pallor | Very Common - Between 80% and 100% cases |
Scarring | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with CYGB gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Optic disc pallor
- Macular degeneration
- Attenuation of retinal blood vessels
- Undetectable electroretinogram
- Macular edema
- Bone spicule pigmentation of the retina
- Bull's eye maculopathy
- Macular scar
And 1 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to CYGB gene
Here you will find a list of rare diseases related to the CYGB. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
RETINITIS PIGMENTOSA 36; RP36
Most common symptoms of RETINITIS PIGMENTOSA 36; RP36
- Cataract
- Edema
- Rod-cone dystrophy
- Pallor
- Scarring
More info about RETINITIS PIGMENTOSA 36; RP36
Search interest in CYGB
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like HSD17B4 COL5A2 ANLN HNRNPH2 PSENEN KCNQ3 FIBP