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Summary Literature (0)
MIM:610706 - DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA

Xenbase Genes: fgf3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012541 - deafness with labyrinthine aplasia, microtia, and microdontia