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Summary Literature (0)
DOID:0060231 - Bruck syndrome


Disease Ontology Definition:A syndrome characterized by a combination of multiple joint contractures and osteogenesis imperfecta.

Synonyms: osteogenesis imperfecta with congenital joint contractures

Xenbase Genes : plod2, fkbp10

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0017195 - Bruck syndrome

OMIM:
OMIM:609220 - BRUCK SYNDROME 2; BRKS2

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

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