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Disease Ontology Browser
Usher syndrome type 1F (DOID:0110832)
Alliance: disease page
Synonyms: USH1F; Usher syndrome type IF
Alt IDs: OMIM:602083, ICD10CM:H35.5
Definition: An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q.

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
12/03/2019
MGI 6.14
The Jackson Laboratory