Disease-gene associations mined from literature

Human genes for dentin dysplasia

Dentin dysplasia [DOID:701]

Dentin dysplasia is a genetic disorder of teeth, commonly exhibiting an autosomal dominant inheritance. It is characterized by presence of normal enamel but atypical dentin with abnormal pulpal morphology. There are two types. Type I is the radicular type, and type II is the coronal type. In the radicular type, the roots of teeth are shorter than normal and the pulp chamber may be nearly gone. The pulp chamber is sometimes described as having a "crescent shaped" appearance. In the coronal type, the pulps are enlarged and are described as having a "thistle tube" appearance, in permanent dentition. In the deciduous dentition, coronal dentin dysplasia bears a resemblance to Dentinogenesis Imperfecta type II.

Synonyms:  dentin dysplasia,  DOID:701,  Dentin dysplasia (disorder),  Dentinal dysplasia,  Dentin dysplasia disorder ...

Linkouts:  OMIM #1 #2