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DOID:0110341 - osteogenesis imperfecta type 2
Disease Ontology Definition:An osteogenesis imperfecta that is characterized by bone fragility and perinatal lethality and has_material_basis_in dominantly inherited mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.
Synonyms: OI2, Vrolik type of osteogenesis imperfecta, osteogenesis imperfecta type II, perinatal lethal osteogenesis imperfecta congenita,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0008147 - osteogenesis imperfecta type 2 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee