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Disease Ontology Browser
Usher syndrome type 3A (DOID:0110841)
Alliance: disease page
Synonyms: USH3A; Usher syndrome type IIIA
Alt IDs: OMIM:276902, ICD10CM:H35.5
Definition: An Usher syndrome type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the CLRN1 gene on chromosome 3q25.

Disease References using Mouse Models (3)

Contributing Projects:
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