Retinitis pigmentosa 38

MONDO:0013469

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

Also known as: MERTK retinitis pigmentosa, RP38, retinitis pigmentosa 38, retinitis pigmentosa caused by mutation in MERTK, retinitis pigmentosa type 38, Rod-cone dystrophy, childhood-onset

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 38 itself.

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Part of

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

Including sub-types (25) Tagged with Retinitis pigmentosa 38 (0)

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