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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, 1 tagged with Usher syndrome type 1G itself.

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↑ Usher syndrome type 1 (3)

Including sub-types (1) Tagged with Usher syndrome type 1G (1)

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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

Usher syndrome type 1G

Where it sits in the disease tree

Newborn screening study aims to catch rare diseases at birth