Usher syndrome type 1G

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Summary

Literature (0)

DOID:0110834 - Usher syndrome type 1G

Disease Ontology Definition:An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25.

Synonyms: USH1G, Usher syndrome type IG

Xenbase 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

: ush1g

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011748 - Usher syndrome type 1G

MONDO:0011748 - Usher syndrome type 1G

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

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

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