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Usher syndrome type 1K

MONDO:0014001

An Usher syndrome type 1 that has material basis in variation in the chromosome region 10p11.21-q21.1.

Also known as: USH1K, USHER syndrome, type IK

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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