Glycine Encephalopathy 2
Disease ID: disease_node_20517
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:620398 |
|---|---|
| Subclassof | DOID_9268 |
| Data Source | DOID |
| Synonyms | GCE2 |
| Doid Label | glycine encephalopathy 2 |
| Doid Description | 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. |
| Disease Node Id | disease_node_20517 |
| Doid Id | DOID_0061001 |
| Label | Glycine Encephalopathy 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Hyperglycinemia, Nonketotic(ID:disease_node_10126) (Disease)