| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://www.omim.org/entry/602080 |
| Similar Terms | |
| Downloads & Tools |
3 genes associated with the paget disease of bone phenotype from the curated OMIM Gene-Disease Associations dataset.
