Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 (DFNA39/DGI1)

Alias:

Dfna39/dentinogenesis Imperfecta 1 Syndrome

Dfna39/dgi1 Syndrome

Dgi1/dfna39 Syndrome

Deafness, Autosomal Dominant, 39, with Dentinogenesis Imperfecta 1

Deafness, Autosomal Dominant, Type 39, with Dentinogenesis

Deafness, Autosomal Dominant 39, with Dentinogenesis

Dfna39/dgi1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1, is also known as dfna39/dentinogenesis imperfecta 1 syndrome, and has symptoms including tinnitus An important gene associated with Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 is DSPP (Dentin Sialophosphoprotein). Related phenotypes are dentinogenesis imperfecta and tinnitus

Related ID：

MALACARDS：DFN355

OMIM：605594

MESH：D003811