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Usher syndrome type 1G

MONDO:0011748

Any Usher syndrome in which the cause of the disease is a mutation in the USH1G gene.

Also known as: USH1G, USH1G Usher syndrome, Usher syndrome caused by mutation in USH1G, Usher syndrome type 1G, USHER syndrome, type Ig, Usher syndrome, type 1G

1 clinical trial 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)

Not yet finished but already full! 1

Newborn screening study aims to catch rare diseases at birth

Diagnosis Ongoing

This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

Sponsor: RTI International • Aim: Diagnosis

Last updated Jul 03, 2026 00:00 UTC