van buchem disease Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A hyperostosis that has_material_basis_in a mutation in the SOST gene which results_in overgrowth of endosteal bone producing dense and wide bones throughout the body especially located_in skull. (Human Disease Ontology, DOID_0080036)
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1 genes associated with the van buchem disease phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SOST sclerostin