Usher syndrome type 3A

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: clrn1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010170 - Usher syndrome type 3A

MONDO:0010170 - Usher syndrome type 3A

MIM:

MIM:276902 - USHER SYNDROME, TYPE IIIA; USH3A

MIM:276902 - USHER SYNDROME, TYPE IIIA; USH3A

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)