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Summary Literature (0)
MIM:103470 - MOVED TO 193510 AND 606952

Xenbase Genes: mitf, tyr

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018138 - ocular albinism with congenital sensorineural hearing loss

Disease Ontology (DO):
DOID:0090100 - ocular albinism with sensorineural deafness