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Summary Literature (0)
DOID:0110338 - osteogenesis imperfecta type 17

Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the SPARC gene on chromosome 5q33.

Synonyms: OI17, osteogenesis imperfecta type XVII

Xenbase Genes : sparc

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014672 - osteogenesis imperfecta type 17


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)