Term Name: amelogenesis imperfecta type 3B
Synonyms:
Definition: An amelogenesis imperfecta type 3 that is characterized by enamel that is reduced in mineral density and is thin, chipped, and absent in places and that has_material_basis_in heterozygous mutation in the amelotin gene.
Ontology: Human Disease [DOID:0080243]   ( DOID:0080243 )

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