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Disease Ontology Browser
amelogenesis imperfecta type 1F (DOID:0110065)
Alliance: disease page
Synonyms: AI1F; amelogenesis imperfecta hypoplastic type IF; amelogenesis imperfecta type IF
Alt IDs: OMIM:616270, ICD10CM:K00.5
Definition: An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the ameloblastin gene (AMBN) on chromosome 4q13.


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
12/03/2019
MGI 6.14
The Jackson Laboratory