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Summary Literature (0)
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: Usher syndrome type I Acadian variety, Usher syndrome type IC, USH1C

Xenbase Genes : ush1c

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010171 - strand of hair of face

MIM:
MIM:276904 - USHER SYNDROME, TYPE IC; USH1C

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): Usher syndrome type 1 (is_a)