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Autosomal dominant rhegmatogenous retinal detachment

MONDO:0016202

Autosomal dominant form of rhegmatogenous retinal detachment.

Also known as: DRRD, rhegmatogenous retinal detachment, autosomal dominant

21 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Eye disorder (97) Retinal disorder (79) Retinal detachment (24) Rhegmatogenous retinal detachment (20) Human disease (14) Hereditary neurological disease (5) Disorder of orbital region (3)
Trials to join now! 15 Not yet recruiting 1 Not yet finished but already full! 1 Completed 3 Terminated 1
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