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Summary Literature (0)
DOID:0110059 - X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2

Disease Ontology Definition:An amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region.

Synonyms: AIH3, X-linked enamel hypoplasia, amelogenesis imperfecta type IE X-linked 2 , amelogenesis imperfecta 3 hypoplastic type,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010522 - X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2


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)