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Disease Ontology Browser
amelogenesis imperfecta type 1C (DOID:0110056)
Alliance: disease page
Synonyms: AI1C; amelogenesis imperfecta type IC; autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion; autosomal recessive amelogenesis imperfecta local hypoplastic type
Alt IDs: ICD10CM:K00.5
Definition: An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the enamelin gene (ENAM).


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
02/11/2020
MGI 6.14
The Jackson Laboratory