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Echinobase
Summary Literature (0)
DOID:0110066 - amelogenesis imperfecta type 1G

Disease Ontology Definition:An amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in the FAM20A gene on chromosome 17q24.

Synonyms: AI1G, AIGFS, amelogenesis imperfecta hypoplastic with nephrocalcinosis, amelogenesis imperfecta type IG, enamel-renal syndrome, enamel-renal-gingival syndrome, ERS, amelogenesis imperfecta and gingival fibromatosis syndrome

Echinobase Genes :


MIM:
MIM:204690 - amelogenesis imperfecta, type ig; ai1g

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): amelogenesis imperfecta (is_a), autosomal recessive disease (is_a)