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amelogenesis imperfecta hypomaturation type 2A3 (DOID:0110061)
Alliance: disease page
Synonyms: AI2A3; amelogenesis imperfecta hypomaturation type IIA3; amelogenesis imperfecta type IIA3
Alt IDs: OMIM:613211, ICD10CM:K00.5
Definition: An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene.

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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Send questions and comments to User Support. 		last database update
01/12/2021
MGI 6.16 		The Jackson Laboratory