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Summary Literature (0)
DOID:0110060 - amelogenesis imperfecta hypomaturation type 2A2


Disease Ontology Definition:An amelogenesis imperfecta that has material basis in homozygous mutation in the matrix metalloproteinase-20 gene (MMP20).

Synonyms: AI2A2, amelogenesis imperfecta hypomaturation type IIA2, amelogenesis imperfecta pigmented hypomaturation type 2, amelogenesis imperfecta type IIA2

Xenbase Genes : mmp20

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012926 - amelogenesis imperfecta hypomaturation type 2A2


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)