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Summary Literature (0)
DOID:0110056 - amelogenesis imperfecta type 1C

Disease Ontology Definition:An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the enamelin gene (ENAM).

Synonyms: amelogenesis imperfecta type IC, AI1C, autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion, autosomal recessive amelogenesis imperfecta local hypoplastic type

Xenbase Genes : enam

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008770 - amelogenesis imperfecta type 1C

MIM:
MIM:204650 - AMELOGENESIS IMPERFECTA, TYPE IC; AI1C

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

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