Usher syndrome type 1H

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Summary

Literature (0)

DOID:0110835 - Usher syndrome type 1H

Disease Ontology Definition:An Usher syndrome type 1 that has_material_basis_in variation in the chromosome region 15q22-q23.

Synonyms: USH1H, Usher syndrome type IH,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): Usher syndrome type 1 (is_a)