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Disease Ontology Browser
amelogenesis imperfecta hypomaturation type 2A2 (DOID:0110060)
Alliance: disease page
Synonyms: AI2A2; amelogenesis imperfecta hypomaturation type IIA2; amelogenesis imperfecta pigmented hypomaturation type 2; amelogenesis imperfecta type IIA2
Alt IDs: OMIM:612529, ICD10CM:K00.5
Definition: An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the matrix metalloproteinase-20 gene (MMP20).

Disease References using Mouse Models (1)

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