Retinitis pigmentosa 46

MONDO:0012943

Any retinitis pigmentosa in which the cause of the disease is a mutation in the IDH3B gene.

Also known as: IDH3B retinitis pigmentosa, RP46, retinitis pigmentosa 46, retinitis pigmentosa caused by mutation in IDH3B, retinitis pigmentosa type 46, retinitis pigmentosa, autosomal recessive, Idh3B-related

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 46 itself.

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Part of

↑ Retinitis pigmentosa (89) ↑ IDH3B-related retinopathy (0)

Including sub-types (25) Tagged with Retinitis pigmentosa 46 (0)

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