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: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

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

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

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