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Echinobase
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 hypomaturation type IIA3, amelogenesis imperfecta type IIA3,

Echinobase Genes :


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

Other Model Organisms: AGR, 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)