| Metadata | |
|---|---|
| ID | DOID:0061001 |
| PURL | http://purl.obolibrary.org/obo/DOID_0061001 Copy |
| Name | glycine encephalopathy 2 |
| Definition | A glycine encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the AMT gene, which encodes a member of the glycine cleavage system (protein T), on chromosome 3p21. https://pubmed.ncbi.nlm.nih.gov/8005589/ |
| Xrefs | |
| Synonyms |
GCE2 [EXACT] |
| Parent Relationships |