CNGB3-related retinopathy

MONDO:0100446

A retinopathy caused by biallelic variants in the CNGB3 gene.

Also known as: CNGB3 retinopathy, ACHM1, ACHM1 (formerly), ACHM1, formerly, ACHM3, CNGB3 achromatopsia, RMCH1, RMCH1 (formerly)

0 clinical trials for this condition and its sub-types, 0 tagged with CNGB3-related retinopathy itself.

Where it sits in the disease tree

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Sub-types of CNGB3-related retinopathy

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