Usher syndrome, type 1D/F

MONDO:0100050

Any Usher syndrome in which the cause of the disease is a mutation in the CDH23 and PCDH15 genes.

Also known as: Usher syndrome, type 1D/F, CDH23/PCDH15, digenic, USH1D/F, CDH23/PCDH15, digenic

0 clinical trials for this condition and its sub-types, 0 tagged with Usher syndrome, type 1D/F itself.

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