"AI1G"@en . "amelogenesis imperfecta type 1G"^^ . _:vb50942444 . _:vb50942444 . "amelogenesis imperfecta hypoplastic with nephrocalcinosis"@en . "ICD10CM:K00.5"^^ . "ORDO:1031"^^ . . . _:vb50942444 . "amelogenesis imperfecta type IG"@en . "enamel-renal syndrome"@en . "enamel-renal-gingival syndrome"@en . _:vb50942444 . "OMIM:204690"^^ . "amelogenesis imperfecta and gingival fibromatosis syndrome"@en . "disease_ontology"^^ . "An amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in the FAM20A gene on chromosome 17q24."^^ . . . "DOID:0110066"^^ . _:vb50942444 . "ERS"@en . "AIGFS"@en .