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Disease Ontology Browser
amelogenesis imperfecta type 1A (DOID:0110054)
Alliance: disease page
Synonyms: AI1A; amelogenesis imperfecta hypoplastic type IA; amelogenesis imperfecta type IA
Alt IDs: OMIM:104530, ICD10CM:K00.5
Definition: An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the beta-3 laminin gene (LAMB3) on chromosome 1q32.

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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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory