Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110832 - Usher syndrome type 1F

Disease Ontology Definition:An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q.

Synonyms: USH1F, Usher syndrome type IF,

Xenbase Genes : pcdh15

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011186 - Usher syndrome type 1F


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Usher syndrome type 1 (is_a)