Usher syndrome type 2D

MONDO:0012662

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

Also known as: USH2D, Usher syndrome caused by mutation in WHRN, Usher syndrome type 2D, WHRN Usher syndrome, USHER syndrome, type IID, Usher syndrome, type 2D

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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) Usher syndrome type 2 (1) Autosomal genetic disease (0) Disease by body system or component (0)

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