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Echinobase
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,

Echinobase Genes :


OMIM:
MIM:606943 - usher syndrome, type ig; ush1g

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)