osteogenesis imperfecta type 16 Disease Ontology Browser

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Disease Ontology Browser

osteogenesis imperfecta type 16 (DOID:0110345)
Alliance: disease page
Synonyms: chromosome 11p11.2 deletion syndrome 91.3-KB; OI16; osteogenesis imperfecta type XVI
Alt IDs: OMIM:616229, ICD10CM:Q78.0
Definition: An osteogenesis imperfecta that has_material_basis_in contiguous gene deletion on chromosome 11p11.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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