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Summary Literature (0)
DOID:0110351 - osteogenesis imperfecta type 11

Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the FKBP10 gene on chromosome 17q21.

Synonyms: OI11, osteogenesis imperfecta type XI

Xenbase Genes : fkbp10

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012592 - osteogenesis imperfecta type 11

MIM:
MIM:610968 - OSTEOGENESIS IMPERFECTA, TYPE XI; OI11

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), osteogenesis imperfecta (is_a)