| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A serine deficiency that has_material_basis_in deficiency of phosphoserine aminotransferase and is characterized by low concentartions of serine and flycine in plasma and cerebrospinal fluid. (Human Disease Ontology, DOID_0050723) |
| External Link | http://www.omim.org/entry/610992 |
| Similar Terms | |
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1 genes associated with the ?phosphoserine aminotransferase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| PSAT1 | phosphoserine aminotransferase 1 |
