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Disease Ontology Browser
Usher syndrome type 2 (DOID:0110827)
Alliance: disease page
Synonyms: USH2
Alt IDs: MESH:D052245, NCI:C126328, ORDO:231178
Definition: An Usher syndrome characterized by mild to severe congenital hearing impairment, normal vestibular function and later development of retinitis pigmentosa.

Disease References using Mouse Models (8)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/12/2024
MGI 6.23
The Jackson Laboratory