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Echinobase
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

Echinobase Genes : whrn


MIM:
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)