Conditions / Genetic
amelogenesis imperfecta type 3A
info · Genetic · ICD-10: K00.5
An amelogenesis imperfecta type 3 that has_material_basis_in heterozygous mutation in the FAM83H gene on chromosome 8q24.
Signs and symptoms
- Amelogenesis imperfecta
- Anterior open-bite malocclusion
- Dental malocclusion
Also known as: ADHCAI; amelogenesis imperfecta hypomineralization type; amelogenesis imperfecta type III; autosomal dominant amelogenesis imperfecta hypocalcification type