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Summary Literature (1)
DOID:0110826 - Usher syndrome type 1


Disease Ontology Definition:An Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa.

Synonyms: US1, USH1

Xenbase Genes : myo7a, cdh23, cib2, pcdh15, ush1g, ush1c

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010168 - Usher syndrome type 1

OMIM:
OMIM:276900 - USHER SYNDROME, TYPE I; USH1

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Usher syndrome (is_a)