X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 Disease Ontology Browser

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Disease Ontology Browser

X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 (DOID:0110059)
Alliance: disease page
Synonyms: AIH3; amelogenesis imperfecta 3 hypoplastic type; amelogenesis imperfecta type IE X-linked 2; X-linked enamel hypoplasia
Alt IDs: OMIM:301201, ICD10CM:K00.5
Definition: An amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region.

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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