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Usher syndrome type 1B (DOID:0070655)
Alliance: disease page
Synonyms: USH1B; Usher syndrome type IB
Alt IDs: OMIM:276900, MESH:C536485, UMLS_CUI:C2931206
Definition: An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the MYO7A gene on chromosome 11q13.

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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12/30/2025
MGI 6.24 		The Jackson Laboratory