Conditions / Genetic
X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
info · Genetic · ICD-10: K00.5
An amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region.
Signs and symptoms
- Amelogenesis imperfecta
Also known as: AIH3; amelogenesis imperfecta 3 hypoplastic type; amelogenesis imperfecta type IE X-linked 2