| Disease Aliases (26) | Ai1g Aigfs Amelogenesis imperfecta and gingival fibromatosis syndrome Amelogenesis imperfecta, hypoplastic, and nephrocalcinosis Amelogenesis imperfecta, hypoplastic, with nephrocalcinosis Absent enamel, nephrocalcinosis and apparently normal calcium metabolism Amelogenesis imperfecta, type ig Amelogenesis imperfecta and nephrocalcinosis Amelogenesis imperfecta hypoplastic type, ig Amelogenesis imperfecta nephrocalcinosis Amelogenesis imperfecta, nephrocalcinosis and impaired renal concentration Amelogenesis imperfecta-gingival hyperplasia syndrome Amelogenesis imperfecta-nephrocalcinosis syndrome Enamel-renal syndrome Enamel-renal-gingival syndrome Ers Enamel renal syndrome Fam20a amelogenesis imperfecta Generalized enamel hypoplasia and renal dysfunction Mcgibbon lubinsky syndrome Amelogenesis imperfecta caused by mutation in fam20a Amelogenesis imperfecta hypoplastic with nephrocalcinosis Amelogenesis imperfecta type 1g Amelogenesis imperfecta type ig Amelogenesis imperfecta, type 1g Amelogenesis imperfecta, type ig; ai1g |
Associated Genes (1) NCBI-RefSeq: FAM20A (FAM20A golgi associated secretory pathway pseudokinase) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Amelogenesis imperfecta type 1G | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |