Usher syndrome type 1G
MONDO:0011748Mondo
Findings
No curated finding names Usher syndrome type 1G yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any Usher syndrome in which the cause of the disease is a mutation in the USH1G gene.
Definition from the Mondo Disease Ontology (MONDO:0011748), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- USH1GHGNC:16356
- Definitive · Laboratory for Molecular Medicine · Autosomal recessive · 2020
- Definitive · G2P · Autosomal recessive · 2025
- Strong · Ambry Genetics · Autosomal recessive · 2019
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2018
- Strong · PanelApp Australia · Autosomal recessive · 2025
Where it sits
- A kind of
Other names
3 names
Resolves to: Usher syndrome type 1G
- Also called
- USH1GUSH1G Usher syndromeUsher syndrome caused by mutation in USH1G