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:0110346 - osteogenesis imperfecta type 10

Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINH gene on chromosome 11q13.

Synonyms: OI10, osteogenesis imperfecta type X,

Xenbase Genes : serpinh1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013459 - osteogenesis imperfecta type 10


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

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