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otospondylomegaepiphyseal dysplasia, autosomal dominant (DOID:0080677)
Alliance: disease page
Alt IDs: OMIM:184840
Definition: An osteochondrodysplasia that is characterized by by autosomal dominant inheritance of mutations in the COL11A2 gene.


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
11/12/2024
MGI 6.24
The Jackson Laboratory