Brown-Vialetto-Van Laere syndrome

Summary

DOID:0050694 - Brown-Vialetto-Van Laere syndrome

Disease Ontology Definition:A syndrome that is characterized by sensorineural hearing loss and a variety of cranial nerve palsies, usually involving the motor components of the seventh and ninth to twelfth cranial nerves.

Synonyms:

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

: slc52a3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008891 - riboflavin transporter deficiency

MONDO:0008891 - riboflavin transporter deficiency

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), autosomal recessive disease (is_a), syndrome (is_a)