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 )

Relationships
is a type of: amelogenesis imperfecta type 3 autosomal dominant disease