Purine-Pyrimidine Metabolic Disorder
Disease ID: disease_node_17499
Connections displayed (default: 10).
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| Dbxref | ICD10CM:E79.8, ICD9CM:277.2, SNOMEDCT_US_2023_03_01:190917005, UMLS_CUI:C0029595 |
|---|---|
| Subclassof | DOID_655 |
| Data Source | DOID |
| Synonyms | inborn errors of purine-pyrimidine metabolism |
| Doid Label | purine-pyrimidine metabolic disorder |
| Doid Description | An inherited metabolic disorder involving dysfunction of purine and pyrimidine metabolism. |
| Disease Node Id | disease_node_17499 |
| Doid Id | DOID_653 |
| Label | Purine-Pyrimidine Metabolic Disorder |
- Incoming r'ship
SUBCLASS_OFto/from Xanthinuria(ID:disease_node_17500) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Metabolism, Inborn Errors(ID:disease_node_5171) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Lesch-Nyhan Syndrome(ID:disease_node_4642) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Dihydropyrimidine Dehydrogenase Deficiency(ID:disease_node_11819) (Disease)