Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

CNGA3-related retinopathy

MONDO:0800102

A retinopathy, typically described as achromatopsia, caused by biallelic variants in the CNGA3 gene.

Also known as: CNGA3-related retinopathy, ACHM2, CNGA3 achromatopsia, RMCH2, achromatopsia 2, achromatopsia caused by mutation in CNGA3, achromatopsia type 2, rod monochromacy 2

25 clinical trials for this condition and its sub-types, 0 tagged with CNGA3-related retinopathy itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Sub-types of CNGA3-related retinopathy

Sort by