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Disease Ontology Browser
osteogenesis imperfecta type 10 (DOID:0110346)
Alliance: disease page
Synonyms: OI10; osteogenesis imperfecta type X
Alt IDs: OMIM:613848, ICD10CM:Q78.0
Definition: An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINH gene on chromosome 11q13.

Disease References using Mouse Models (1)

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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last database update
MGI 6.19
The Jackson Laboratory