| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An amino acid metabolic disorder that involves abnormally high levels of the amino acid glycine in bodily fluids and tissues. (Human Disease Ontology, DOID_9268) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0008288 |
| Similar Terms | |
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1 genes associated with the nonketotic hyperglycinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| GLYCTK | glycerate kinase |
