Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 68934012 | Classical galactosemia, heterozygous type | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 492965019 | Classical galactosaemia, heterozygous type | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 778102012 | Classical galactosemia, heterozygous type (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Classical galactosemia, heterozygous type | Is a | Deficiency of UTP-hexose-1-phosphate uridylyltransferase | false | Inferred relationship | Existential restriction modifier | ||
| Classical galactosemia, heterozygous type | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Classical galactosemia, heterozygous type | Is a | Deficiency of uridine triphosphate-hexose-1-phosphate uridylyltransferase | true | Inferred relationship | Existential restriction modifier | ||
| Classical galactosemia, heterozygous type | Causative agent | Uridine triphosphate-hexose-1-phosphate uridylyltransferase | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR