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Metadata
ID	DOID:0080243
Name	amelogenesis imperfecta type 3B
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. https://pubmed.ncbi.nlm.nih.gov/27412008/
Xrefs	MIM:617607
Parent Relationships	is_a autosomal dominant disease is_a amelogenesis imperfecta type 3
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance