amelogenesis imperfecta hypomaturation type 2A3

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Summary

Literature (0)

DOID:0110061 - amelogenesis imperfecta hypomaturation type 2A3

Disease Ontology Definition:An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene.

Synonyms: AI2A3, amelogenesis imperfecta type IIA3, amelogenesis imperfecta hypomaturation type IIA3

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

MIM:

MIM:613211 - amelogenesis imperfecta, hypomaturation type, iia3; ai2a3

MIM:613211 - amelogenesis imperfecta, hypomaturation type, iia3; ai2a3

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): amelogenesis imperfecta (is_a), autosomal recessive disease (is_a)