| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An osteosclerosis that has_material_basis_in mutations in the TGFB1 gene which results_in increased bone density located_in long bone. (Human Disease Ontology, DOID_4997) |
| External Link | http://www.omim.org/entry/131300 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the camurati-engelmann disease phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| TGFB1 | transforming growth factor, beta 1 |
