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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,
Echinobase Genes : pcdh15
MIM:601067 - usher syndrome, type id; ush1d usher syndrome, type id/f, cdh23/pcdh15, digenic, included;; ush1d/f, cdh23/pcdh15, digenic, included |
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)