Usher syndrome type 2D

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Summary

Literature (0)

DOID:0110840 - Usher syndrome type 2D

Disease Ontology Definition:An Usher syndrome type 2 that has_material_basis_in by homozygous or compound heterozygous mutation in the WHRN gene on chromosome 9q32.

Synonyms: USH2D, Usher syndrome type IID

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

: whrn

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012662 - Usher syndrome type 2D

MONDO:0012662 - Usher syndrome type 2D

MIM:

MIM:611383 - USHER SYNDROME, TYPE IID; USH2D

MIM:611383 - USHER SYNDROME, TYPE IID; USH2D

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

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

Parent(s): Usher syndrome type 2 (is_a)