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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
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0008770 - amelogenesis imperfecta type 1C |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee