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Disease Ontology Browser
Usher syndrome type 1 (DOID:0110826)
Alliance: disease page
Synonyms: US1; USH1
Alt IDs: OMIM:276900, ICD10CM:H35.5, ORDO:231169
Definition: An Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa.

Disease References using Mouse Models (26)

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
01/24/2023
MGI 6.22
The Jackson Laboratory