Usher syndrome type 1

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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

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

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

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010168 - collection of eyelashes

MONDO:0010168 - collection of eyelashes

MIM:

MIM:276900 - USHER SYNDROME, TYPE I; USH1

MIM:276900 - USHER SYNDROME, TYPE I; USH1

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

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

Parent(s): Usher syndrome (is_a)