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Disease Ontology Browser
Usher syndrome type 1C (DOID:0110830)
Alliance: disease page
Synonyms: USH1C; Usher syndrome type I Acadian variety; Usher syndrome type IC
Alt IDs: OMIM:276904, ICD10CM:H35.5
Definition: An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15.

Disease References using Mouse Models (6)

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
11/14/2017
MGI 6.11
The Jackson Laboratory