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Usher syndrome type 1H

MONDO:0012968

An Usher syndrome type 1 that has material basis in variation in the chromosome region 15q22-q23.

Also known as: USH1H, Usher syndrome, type 1H, USHER syndrome, type IH

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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