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.

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Part of

↑ Inherited retinal dystrophy (513)

Sub-types of CNGA3-related retinopathy

Achromatopsia 2 0 trials

Including sub-types (25) Tagged with CNGA3-related retinopathy (0)

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