RDH12-related recessive retinopathy

MONDO:0800099

A retinopathy, typically severe, and early onset, caused by biallelic variants in the RDH12 gene.

Also known as: RDH12-related recessive retinopathy, LCA13, Leber congenital amaurosis 13, Leber congenital amaurosis caused by mutation in RDH12, Leber congenital amaurosis type 13, RDH12 Leber congenital amaurosis, retinitis pigmentosa 53

25 clinical trials for this condition and its sub-types, 0 tagged with RDH12-related recessive retinopathy itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Inherited retinal dystrophy (513)

Sub-types of RDH12-related recessive retinopathy

Leber congenital amaurosis 13 0 trials

Including sub-types (25) Tagged with RDH12-related recessive retinopathy (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.