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Summary Literature (0)
DOID:0110841 - Usher syndrome type 3A

Disease Ontology Definition:An Usher syndrome type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the CLRN1 gene on chromosome 3q25.

Synonyms: USH3A, Usher syndrome type IIIA

Xenbase Genes : clrn1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010170 - Usher syndrome type 3A


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)