Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Apr 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5035134012 | L-ferritin deficiency (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| 5035135013 | L-ferritin deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 5035136014 | LFTD - L-ferritin deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| L-ferritin deficiency | Is a | Serum ferritin level below reference range | true | Inferred relationship | Existential restriction modifier | ||
| L-ferritin deficiency | Is a | Autosomal hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| L-ferritin deficiency | Interprets | Serum ferritin measurement | true | Inferred relationship | Existential restriction modifier | 1 | |
| L-ferritin deficiency | Has interpretation | Below reference range | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR