osteogenesis imperfecta type 13

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: bmp1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013924 - osteogenesis imperfecta type 13

MONDO:0013924 - osteogenesis imperfecta type 13

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)