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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: AI1C, amelogenesis imperfecta type IC, 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


Other Model Organisms: AGR, 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)