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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, UMLS_CUI:C0339533
Definition: An Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa.

Disease References using Mouse Models (24)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory