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Disease Ontology Browser
Usher syndrome type 1D (DOID:0110831)
Alliance: disease page
Synonyms: USH1D; Usher syndrome type ID
Alt IDs: OMIM:601067, ICD10CM:H35.5
Definition: An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22.

Disease References using Mouse Models (3)

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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last database update
MGI 6.17
The Jackson Laboratory