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Echinobase
Summary Literature (0)
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,

Echinobase Genes : pcdh15, myo7a


OMIM:
MIM: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)