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Summary Literature (0)
DOID:0110054 - amelogenesis imperfecta type 1A

Disease Ontology Definition:An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the beta-3 laminin gene (LAMB3) on chromosome 1q32.

Synonyms: AI1A, amelogenesis imperfecta hypoplastic type IA, amelogenesis imperfecta type IA

Xenbase Genes : lamb3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007094 - amelogenesis imperfecta type 1A


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 dominant disease (is_a)