amelogenesis imperfecta hypomaturation type 2A5 Disease Ontology Browser

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amelogenesis imperfecta hypomaturation type 2A5 (DOID:0110063)
Alliance: disease page
Synonyms: AI2A5; amelogenesis imperfecta hypomaturation type IIA5; amelogenesis imperfecta type IIA5
Alt IDs: OMIM:615887, ICD10CM:K00.5
Definition: An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the SLC24A4 gene on chromosome 14q32.

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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