Usher syndrome type 3B

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Summary

Literature (0)

DOID:0110842 - Usher syndrome type 3B

Disease Ontology Definition:An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31.

Synonyms: USH3B, Usher syndrome type IIIB

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

: hars1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013788 - Usher syndrome type 3B

MONDO:0013788 - Usher syndrome type 3B

MIM:

MIM:614504 - USHER SYNDROME, TYPE IIIB; USH3B

MIM:614504 - USHER SYNDROME, TYPE IIIB; USH3B

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

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

Parent(s): Usher syndrome type 3 (is_a)