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Summary Literature (1)
DOID:0110831 - Usher syndrome type 1D

Disease Ontology Definition:An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22.

Synonyms: USH1D, Usher syndrome type ID,

Xenbase Genes : cdh23, pcdh15

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010984 - Usher syndrome type 1D


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)