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DOID:0110830 - Usher syndrome type 1C
Disease Ontology Definition:An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15.
Synonyms: USH1C, Usher syndrome type I Acadian variety, Usher syndrome type IC,
Echinobase Genes :
MIM:276904 - usher syndrome, type ic; ush1c |
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)