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LA30.6 Amelogenesis imperfecta

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Amelogenesis imperfecta presents with a rare abnormal formation of the enamel or external layer of the crown of teeth. Amelogenesis imperfecta is due to the malfunction of the proteins in the enamel: ameloblastin, enamelin, tuftelin and amelogenin. People afflicted with amelogenesis imperfecta have teeth with abnormal colour: yellow, brown or grey; this disorder can afflict any number of teeth of both dentitions. The teeth have a higher risk for dental cavities and are hypersensitive to temperature changes as well as rapid attrition, excessive calculus deposition, and gingival hyperplasia.

inclusions

• Hypocalcified amelogenesis imperfecta
• Hypomaturation amelogenesis imperfecta

synonyms

• Amelogenesis imperfecta
• AI - [amelogenesis imperfecta]
• Hypocalcified amelogenesis imperfecta
• hypomineralisation amelogenesis imperfecta
• Hypomaturation amelogenesis imperfecta
• Hypomaturation hypoplastic amelogenesis imperfecta with taurodontism
• Hypoplastic amelogenesis imperfecta
• hypoplasia amelogenesis imperfecta
• hereditary enamel hypoplasia
• congenital enamel hypoplasia
• Amelogenesis imperfecta - gingival hyperplasia
• Amelogenesis imperfecta - cone rod dystrophy
• Jalili syndrome
• Amelogenesis imperfecta - nephrocalcinosis

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