| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An osteochondrodysplasia that has_material_basis_in lack of responsiveness to parathyroid hormone which results_in shortening and widening of long bones of the located_in hand or located_in foot along with short stature, obesity, and rounded face. (Human Disease Ontology, DOID_0080053) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537045 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Albright's hereditary osteodystrophy from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| GNAS | GNAS complex locus | 2.88009 |
