|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A bone formation disease that has_material_basis_in hyperactive osteoclast which results_in abnormal osteoblast bone formation located_in skull, located_in pelvis, located_in vertebral column, located_in set of limbs. (Human Disease Ontology, DOID_5408)|
|Downloads & Tools|
3 genes associated with the paget disease of bone phenotype from the curated OMIM Gene-Disease Associations dataset.