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Summary Literature (0)
DOID:0110348 - osteogenesis imperfecta type 12


Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the SP7 gene on chromosome 12q13.

Synonyms: OI12, osteogenesis imperfecta type XII

Xenbase Genes : sp7

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013460 - osteogenesis imperfecta type 12

OMIM:
OMIM:613849 - OSTEOGENESIS IMPERFECTA, TYPE XII; OI12

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)