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Disease Ontology Browser
osteogenesis imperfecta type 20 (DOID:0111849)
Alliance: disease page
Synonyms: OI20; osteogenesis imperfecta type XX
Alt IDs: OMIM:618644
Definition: An osteogenesis imperfecta characterized by osteopenia, skeletal deformity, and both healed and new fractures on radiography that has_material_basis_in homozygous or compound heterozygous mutation in MESD on chromosome 15q25.1.


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
06/23/2022
MGI 6.20
The Jackson Laboratory