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Summary Literature (0)
DOID:0110065 - amelogenesis imperfecta type 1F

Disease Ontology Definition:An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the ameloblastin gene (AMBN) on chromosome 4q13.

Synonyms: AI1F, amelogenesis imperfecta hypoplastic type IF, amelogenesis imperfecta type IF

Xenbase Genes : ambn

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014560 - amelogenesis imperfecta type 1F


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)