CYSLTR2 gene related symptoms and diseases

All the information presented here about the CYSLTR2 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,OMIM,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.

Table of contents:

Main symptoms and clinical features
Other symptoms and clinical features
Related Diseases
Current trends
Suitable testing panels

Top 5 symptoms and clinical features associated to CYSLTR2 gene

Symptoms // Phenotype	% Cases
Neoplasm	Very Common - Between 80% and 100% cases
Metamorphopsia	Very Common - Between 80% and 100% cases
Abnormal visual accommodation	Very Common - Between 80% and 100% cases
Ciliary body melanoma	Very Common - Between 80% and 100% cases
Iris melanoma	Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with CYSLTR2 gene alterations may also develop some of the following symptoms and phenotypes:

Commonly - More than 50% cases
Choroidal melanoma
Inferior lens subluxation
Subretinal fluid
Photopsia
Uveal melanoma
Zonular cataract
Abnormal fundus morphology
Mydriasis

And 13 more phenotypes, you can get all of them using our tools for rare diseases.

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Rare diseases associated to CYSLTR2 gene

Here you will find a list of rare diseases related to the CYSLTR2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.

UVEAL MELANOMA

Alternate names

UVEAL MELANOMA Is also known as choroidal melanoma, iris melanoma

Description

Uveal melanoma is a rare tumor of the eye, arising from the choroid in 90% of cases and from the iris and ciliary body in the other 10% of cases, which clinically presents with visual symptoms (including blurred vision, photopsia, floaters, and visual field reduction), a visible mass and pain. Fatal metastatic disease is seen in about half of all patients, with the liver being the most frequent site of metastasis.