Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2989311014 | Congenital leptin deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2989546019 | Congenital leptin deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital leptin deficiency | est un(e) (attribut) | Congenital disease | true | Inferred relationship | Some | ||
| Congenital leptin deficiency | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Congenital leptin deficiency | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set
REFERS TO concept association reference set
FHIR