RHO-related retinopathy

MONDO:0700380

Any retinopathy caused by a variant in the RHO gene, including cases diagnosed as congenital stationary night blindness autosomal dominant 1 or retinitis pigmentosa 4.

Also known as: RHO-related retinopathy

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

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Where it sits in the disease tree

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Part of

↑ Inherited retinal dystrophy (510)

Sub-types of RHO-related retinopathy

Retinitis pigmentosa 4 5 trials
Congenital stationary night blindness autosomal dominant 1 3 trials

Including sub-types (32) Tagged with RHO-related retinopathy (0)

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