Status: current, 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 |
2530084012 | Hawkinsinuria (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
2533521010 | Hawkinsinuria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hawkinsinuria | Is a | 4-Hydroxyphenylpyruvate dioxygenase deficiency | true | Inferred relationship | Existential restriction modifier | ||
Hawkinsinuria | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Hawkinsinuria | Is a | Disorder of sulfur-bearing amino acid metabolism | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets