Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2005. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1761010 | 4-Hydroxyphenylpyruvate dioxygenase deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 1762015 | Hawkinsinuria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 492536018 | 4-Hydroxyphenylpyruvate hydroxylase deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 492537010 | Tyrosinaemia type III | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 492538017 | Tyrosinemia type III | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 776919015 | 4-Hydroxyphenylpyruvate dioxygenase deficiency (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| 4-Hydroxyphenylpyruvate dioxygenase deficiency | Is a | Enzymopathy | false | Inferred relationship | Existential restriction modifier | ||
| 4-Hydroxyphenylpyruvate dioxygenase deficiency | Is a | Tyrosinuria | false | Inferred relationship | Existential restriction modifier | ||
| 4-Hydroxyphenylpyruvate dioxygenase deficiency | Is a | Disorder of sulfur-bearing amino acid metabolism | false | Inferred relationship | Existential restriction modifier | ||
| 4-Hydroxyphenylpyruvate dioxygenase deficiency | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| 4-Hydroxyphenylpyruvate dioxygenase deficiency | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR