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Summary Literature (0)
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 : slc52a3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008891 - riboflavin transporter deficiency

MIM:
MIM:211530 - BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1

Other Model Organisms: Alliance, 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)