Usher syndrome type 1H Disease Ontology Browser

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Disease Ontology Browser

Usher syndrome type 1H (DOID:0110835)
Alliance: disease page
Synonyms: USH1H; Usher syndrome type IH
Alt IDs: OMIM:612632, ICD10CM:H35.5
Definition: An Usher syndrome type 1 that has_material_basis_in variation in the chromosome region 15q22-q23.

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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