amelogenesis imperfecta type 1G (DOID:0110066)
Alliance: disease page
Synonyms: AI1G; AIGFS; amelogenesis imperfecta and gingival fibromatosis syndrome; amelogenesis imperfecta hypoplastic with nephrocalcinosis; amelogenesis imperfecta type IG; enamel-renal syndrome; enamel-renal-gingival syndrome; ERS
Alt IDs: OMIM:204690, ICD10CM:K00.5, ORDO:1031
Definition: An amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in the FAM20A gene on chromosome 17q24.