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DOID:0110058 - amelogenesis imperfecta type 1E
Disease Ontology Definition:An amelogenesis imperfecta that has_material_basis_in X-linked dominant 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,
Xenbase Genes : amelx
MONDO:0010521 - amelogenesis imperfecta type 1E |
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)