Summary Literature (0)

DOID:0110058 - amelogenesis imperfecta type 1E

Disease Ontology Definition:An amelogenesis imperfecta that has material basis in mutation in the gene encoding amelogenin (AMELX).

Synonyms: AIH1, X-linked amelogenesis imperfecta 1, X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1, X-linked enamel hypoplasia, amelogenesis imperfecta hypomaturationtype with snow-capped teeth, amelogenesis imperfecta type IE,

Echinobase Genes :


OMIM:

MIM:301200 - amelogenesis imperfecta, type ie; ai1e

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee