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Disease Ontology Browser
Usher syndrome type 3B (DOID:0110842)
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.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory