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Summary Literature (0)
DOID:0110350 - osteogenesis imperfecta type 6

Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINF1 gene on chromosome 17p13.3.

Synonyms: OI6, osteogenesis imperfecta type VI

Xenbase Genes : serpinf1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013515 - osteogenesis imperfecta type 6


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

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