| Dataset | OMIM 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://www.omim.org/entry/605899 |
| Similar Terms | |
| Downloads & Tools |
3 genes associated with the glycine encephalopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
