Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3642758018 | Familial benign copper deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3642759014 | Familial benign hypocupremia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3642760016 | Familial benign copper deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3642761017 | Familial benign hypocupraemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial benign copper deficiency | Is a | Hypocupremia | true | Inferred relationship | Existential restriction modifier | ||
| Familial benign copper deficiency | Is a | Hereditary disease | false | Inferred relationship | Existential restriction modifier | ||
| Familial benign copper deficiency | Is a | Disorder of copper metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Familial benign copper deficiency | Is a | Familial disease | true | Inferred relationship | Existential restriction modifier | ||
| Familial benign copper deficiency | Is a | Hereditary metabolic disease | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR