Usher syndrome type 3B Disease Ontology Browser

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Disease Ontology Browser

Usher syndrome type 3B (DOID:0110842)
Alliance: disease page
Synonyms: USH3B; Usher syndrome type IIIB
Alt IDs: OMIM:614504, ICD10CM:H35.5
Definition: An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31.

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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