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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: 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)