usher syndrome Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A syndrome characterized by a combination of hearing loss and visual impairment. (Human Disease Ontology, DOID_0050439)
Similar Terms
Downloads & Tools

Genes

7 genes associated with the disease usher syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
ADGRV1	adhesion G protein-coupled receptor V1
CDH23	cadherin-related 23
CLRN1	clarin 1
MYO7A	myosin VIIA
USH1C	Usher syndrome 1C (autosomal recessive, severe)
USH1G	Usher syndrome 1G (autosomal recessive)
USH2A	Usher syndrome 2A (autosomal recessive, mild)