amelogenesis imperfecta type 3A (DOID:0110055)
Alliance: disease page
Synonyms: ADHCAI; amelogenesis imperfecta hypomineralization type; amelogenesis imperfecta type III; autosomal dominant amelogenesis imperfecta hypocalcification type
Alt IDs: OMIM:130900, ICD10CM:K00.5
Definition: An amelogenesis imperfecta type 3 that has_material_basis_in heterozygous mutation in the FAM83H gene on chromosome 8q24.