RAB28-related retinopathy

MONDO:0100448

A retinopathy caused by biallelic variants in the RAB28 gene.

Also known as: RAB28 retinopathy, CORD18, RAB28 cone-rod dystrophy, cone-rod dystrophy 18, cone-rod dystrophy caused by mutation in RAB28, cone-rod dystrophy type 18

25 clinical trials for this condition and its sub-types, 0 tagged with RAB28-related retinopathy itself.

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↑ Inherited retinal dystrophy (513)

Sub-types of RAB28-related retinopathy

Cone-rod dystrophy 18 0 trials

Including sub-types (25) Tagged with RAB28-related retinopathy (0)

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