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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