Usher syndrome type 3

Summary
Synonym
  • USH3
Definition
An Usher syndrome characterized by progressive hearing loss typically beginning in late childhood, variable vestibular dysfunction and onset of retinitis pigmentosa by the second decade of life.
Super Class
Usher syndrome
Disease Ontology
DOID:0110828
Mondo Disease Ontology
MeSH
NCI Thesaurus
ORDO
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7401 CLRN1 clarin 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
229320 Clrn1 clarin 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024