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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 (7)
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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12/10/2024
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