Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3313334013 | Congenital analbuminemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3313335014 | Congenital analbuminemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3313336010 | Congenital analbuminaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital analbuminemia | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier | ||
| Congenital analbuminemia | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Congenital analbuminemia | Is a | Hypoalbuminemia | true | Inferred relationship | Existential restriction modifier | ||
| Congenital analbuminemia | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR