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Summary Literature (0)
DOID:0110336 - osteogenesis imperfecta type 8

Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the P3H1 gene on chromosome 1p34.2.

Synonyms: OI8, osteogenesis imperfecta type VIII

Xenbase Genes : p3h1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012581 - osteogenesis imperfecta type 8


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)