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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


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)