Conditions / Genetic
amelogenesis imperfecta type 1B
info · Genetic · ICD-10: K00.5
An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the enamelin gene (ENAM) on chromosome 4q13.
Signs and symptoms
- Amelogenesis imperfecta
Also known as: AI1B; AIH2; amelogenesis imperfecta type IB; autosomal dominant hypoplastic local amelogenesis imperfecta; hereditary localized enamel hypoplasia