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Echinobase
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,

Echinobase Genes : pcdh15


OMIM:
MIM:602083 - usher syndrome, type if; ush1f

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)