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deafness, autosomal dominant 39, with dentinogenesis imperfecta 1

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description A disorder characterized by the association of progressive sensorineural high-frequency hearing loss with dentinogenesis imperfecta.
Mondo Term and Equivalent IDs
MONDO:0011571:  deafness, autosomal dominant 39, with dentinogenesis imperfecta 1
MESH:C565316: 
UMLS:C1854146: