Tyrosinemia
Disease ID: disease_node_13245
Connections displayed (default: 10).
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| Dbxref | ICD10CM:E70.21, SNOMEDCT_US_2023_03_01:190694001, UMLS_CUI:C0268483 |
|---|---|
| Subclassof | DOID_9252 |
| Data Source | DOID |
| Doid Label | tyrosinemia |
| Doid Description | An amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine. OMIM mapping submitted by NeuroDevNet. [LS]. |
| Disease Node Id | disease_node_13245 |
| Doid Id | DOID_9275 |
| Label | Tyrosinemia |
- Outgoing r'ship
SUBCLASS_OFto/from Amino Acid Metabolism, Inborn Errors(ID:disease_node_1143) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Tyrosinemia Type Iii(ID:disease_node_13246) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Tyrosinemia Type Ii(ID:disease_node_13248) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Tyrosinemia Type I(ID:disease_node_13247) (Disease)