|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Albright's hereditary osteodystrophy from the curated CTD Gene-Disease Associations dataset.
|GNAS||GNAS complex locus||2.88009|