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Disease Ontology Browser
Usher syndrome type 2D (DOID:0110840)
Synonyms: USH2D; Usher syndrome type IID
Alt IDs: OMIM:611383, ICD10CM:H35.5
Definition: An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32.

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
09/12/2017
MGI 6.10
The Jackson Laboratory