| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://www.omim.org/entry/601815 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the phosphoglycerate dehydrogenase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| PHGDH | phosphoglycerate dehydrogenase |
