Usher syndrome type 2

Summary
Synonym
  • USH2
Definition
An Usher syndrome characterized by mild to severe congenital hearing impairment, normal vestibular function and later development of retinitis pigmentosa.
Super Class
Usher syndrome
Disease Ontology
DOID:0110827
Mondo Disease Ontology
MeSH
NCI Thesaurus
ORDO
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7399 USH2A usherin
Displaying 1 entry
Gene ID Gene Symbol Description Source
22283 Ush2a usherin

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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