| Term Name: | glycine encephalopathy 1 |
|---|---|
| Synonyms: | GCE1 |
| Definition: | A glycine encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the GLDC gene, a member of the mitochondrial glycine cleavage system that encodes the P protein, on chromosome 9p24. |
| Ontology: | Human Disease [DOID:0070616] ( DOID:0070616 ) |