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Disease Ontology Browser
Baller-Gerold syndrome (DOID:0050654)
Alliance: disease page
Alt IDs: OMIM:218600, MESH:C536788, ORDO:1223, UMLS_CUI:C0265308
Definition: A synostosis characterized by coronal craniosynostosis, short stature, and aplasia or hypoplasia of the radial bone.


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
11/05/2024
MGI 6.24
The Jackson Laboratory