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Summary Literature (0)
DOID:0110344 - osteogenesis imperfecta type 5

Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the IFITM5 gene on chromosome 11p15.

Synonyms: OI5, osteogenesis imperfecta type V

Xenbase Genes : ifitm5

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012591 - osteogenesis imperfecta type 5


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

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