Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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: 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)