|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A serine deficiency that has_material_basis_in deficiency of phosphoglycerate dehydrogenase which results in a disruption of L-serine biosynthesis. (Human Disease Ontology, DOID_0050722)|
|Downloads & Tools|
1 genes associated with the phosphoglycerate dehydrogenase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.