/deafness, autosomal dominant 39, with dentinogenesis imperfecta 1

deafness, autosomal dominant 39, with dentinogenesis imperfecta 1

Rare Disease

MONDO:0011571

Also Known As

deafness, autosomal dominant 39, with dentinogenesis imperfecta 1deafness, autosomal dominant 39, with dentinogenesis imperfecta type 1deafness, autosomal dominant 39, with dentinogenesisDfna39/Dgi1 syndromeDfna39/dentinogenesis imperfecta 1 syndromeDgi1/Dfna39 syndrome

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Associated Genes

DSPP ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:605594 ↗

GARD

GARD:15383 ↗

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