| Term Name: | amelogenesis imperfecta type 3A |
|---|---|
| Synonyms: | ADHCAI, AI3, amelogenesis imperfecta hypomineralization type, amelogenesis imperfecta type III, autosomal dominant amelogenesis imperfecta hypocalcification type |
| Definition: | An amelogenesis imperfecta type 3 that has_material_basis_in heterozygous mutation in the FAM83H gene on chromosome 8q24. |
| Ontology: | Human Disease [DOID:0110055] ( DOID:0110055 ) |