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Summary Literature (0)
DOID:0080243 - amelogenesis imperfecta type 3B

Disease Ontology Definition:An amelogenesis imperfecta type 3 that is characterized by enamel that is reduced in mineral density and is thin, chipped, and absent in places and that has_material_basis_in heterozygous mutation in the amelotin gene.

Synonyms:

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0021547 - amelogenesis imperfecta type 3B


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): amelogenesis imperfecta type 3 (is_a), autosomal dominant disease (is_a)