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Summary Literature (0)
DOID:0110342 - osteogenesis imperfecta type 13

Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the BMP1 gene on chromosome 8p21.

Synonyms: OI13, osteogenesis imperfecta type XIII

Xenbase Genes : bmp1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013924 - osteogenesis imperfecta type 13

MIM:
MIM:614856 - OSTEOGENESIS IMPERFECTA, TYPE XIII; OI13

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)