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Disease Ontology Browser
Usher syndrome type 1J (DOID:0110836)
Alliance: disease page
Synonyms: USH1J; Usher syndrome type IJ
Alt IDs: OMIM:614869, ICD10CM:H35.5
Definition: An Usher syndrome type 1 that has_material_basis_in caused by homozygous mutation in the CIB2 gene on chromosome 15q24.

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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MGI 6.19
The Jackson Laboratory