Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 102092012 | Classical galactosemia, homozygous Negro-type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 499013017 | Classical galactosaemia, homozygous Negro-type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 800515019 | Classical galactosemia, homozygous Negro-type (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Classical galactosaemia, homozygous Negro-type | Is a | Deficiency of UTP-hexose-1-phosphate uridylyltransferase | true | Inferred relationship | Some | ||
| Classical galactosaemia, homozygous Negro-type | Causative agent | UTP-hexose-1-phosphate uridylyltransferase | true | Inferred relationship | Some | 1 | |
| Classical galactosaemia, homozygous Negro-type | Is a | Deficiency of UTP-hexose-1-phosphate uridylyltransferase | false | Inferred relationship | Some | ||
| Classical galactosaemia, homozygous Negro-type | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR