Usher syndrome type 3A

MONDO:0010170

Any Usher syndrome in which the cause of the disease is a mutation in the CLRN1 gene.

Also known as: CLRN1 Usher syndrome, USH3A, Usher syndrome caused by mutation in CLRN1, Usher syndrome type 3A, USHER syndrome, type IIIA, Usher syndrome, type 3, Usher syndrome, type 3A

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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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