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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.

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Broader categories

Disease (618) Hereditary disease (172) Syndromic disease (24) Human disease (14) Usher syndrome (12) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Autosomal genetic disease (0) Disease by body system or component (0) Disease by etiologic mechanism (0)

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