Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3307237014 | Congenital deficiency of alpha-fetoprotein (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3307238016 | Congenital deficiency of alpha-fetoprotein | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital deficiency of alpha-fetoprotein | Is a | Congenital disease | true | Inferred relationship | Some | ||
| Congenital deficiency of alpha-fetoprotein | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Congenital deficiency of alpha-fetoprotein | Is a | Alpha-fetoprotein low | true | Inferred relationship | Some | ||
| Congenital deficiency of alpha-fetoprotein | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital deficiency of alpha-fetoprotein | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
| Congenital deficiency of alpha-fetoprotein | Interprets | Alpha-1-Fetoprotein measurement | true | Inferred relationship | Some | 2 |
| 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