Usher syndrome type 1F

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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 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

: pcdh15

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011186 - Usher syndrome type 1F

MONDO:0011186 - Usher syndrome type 1F

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

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

Parent(s): Usher syndrome type 1 (is_a)