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amelogenesis imperfecta type 1E (DOID:0110058)
Alliance: disease page
Synonyms: AIH1; amelogenesis imperfecta hypomaturationtype with snow-capped teeth; amelogenesis imperfecta type IE; X-linked amelogenesis imperfecta 1; X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1; X-linked enamel hypoplasia
Alt IDs: OMIM:301200, ICD10CM:K00.5
Definition: An amelogenesis imperfecta that has material basis in mutation in the gene encoding amelogenin (AMELX).

Disease References using Mouse Models (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory