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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
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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