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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 : whrn

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012662 - Usher syndrome type 2D


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Usher syndrome type 2 (is_a)