Chapter 11 - Diseases of the digestive system (K00-K95)»Diseases of oral cavity and salivary glands (K00-K14)»Hereditary disturbances in tooth structure, not elsewhere classified (K00.5)
K00.5
Hereditary disturbances in tooth structure, not elsewhere classified
Related indications (MeSH) (2)
Amelogenesis Imperfecta1 drug (1 experimental)
A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION.
An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed)