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Summary Literature (0)
MIM:605594 - DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1

Xenbase Genes: dspp

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007441 - dentinogenesis imperfecta type 2
MONDO:0011571 - deafness, autosomal dominant 39, with dentinogenesis imperfecta 1