Conditions / Genetic
amelogenesis imperfecta type 1F
info · Genetic · ICD-10: K00.5
An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the ameloblastin gene (AMBN) on chromosome 4q13.
Signs and symptoms
- Abnormality of dental color
- Amelogenesis imperfecta
- Enamel hypoplasia
- Dental enamel pits
Also known as: AI1F; amelogenesis imperfecta hypoplastic type IF; amelogenesis imperfecta type IF