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DOID:0110842 - Usher syndrome type 3B
Disease Ontology Definition:An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31.
Synonyms: USH3B, Usher syndrome type IIIB
Echinobase Genes : LOC105444109
MIM:614504 - usher syndrome, type iiib; ush3b |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Usher syndrome type 3 (is_a)