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Summary Literature (0)
DOID:0110337 - osteogenesis imperfecta type 7

Disease Ontology Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the CRTAP gene on chromosome 3p22.

Synonyms: OI7, osteogenesis imperfecta type VII

Xenbase Genes : crtap

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012536 - osteogenesis imperfecta type 7


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)