D003811Level 5
Dentinogenesis Imperfecta
**Definition:** An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops poorly with low mineral content while the pulp canal is obliterated.
**Tree numbers:** - C07.650.800.270 - C07.793.700.270 - C16.131.850.800.270
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