Hyperglycinemia, Nonketotic
Disease ID: disease_node_10126
Connections displayed (default: 10).
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| Dbxref | GARD:7219, ICD10CM:E72.51, MESH:D020158, MIM:PS605899, NCI:C84937, ORDO:407, SNOMEDCT_US_2023_03_01:237939006, UMLS_CUI:C0751748 |
|---|---|
| Subclassof | DOID_0050737, DOID_9252 |
| Data Source | DOID, MESH |
| Synonyms | GCE, NKH, Non-ketotic hyperglycinemia, nonketotic hyperglycinemia |
| Mesh Id | D020158 |
| Mesh Label | Hyperglycinemia, Nonketotic |
| Mesh Subclassof | D020739, D000592 |
| Doid Label | glycine encephalopathy |
| Doid Description | An amino acid metabolic disorder that involves abnormally high levels of the amino acid glycine in bodily fluids and tissues. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_10126 |
| Doid Id | DOID_9268 |
| Label | Hyperglycinemia, Nonketotic |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Amino Acid Metabolism, Inborn Errors(ID:disease_node_1143) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Glycine Encephalopathy 1(ID:disease_node_20516) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Glycine Encephalopathy 2(ID:disease_node_20517) (Disease)