Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3322216019 | Deficiency of cathepsin D (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3322217011 | Deficiency of cathepsin D | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3322218018 | Cathepsin D deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Deficiency of cathepsin D | Is a | Specific enzyme deficiency | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital neuronal ceroid lipofuscinosis | Due to | True | Deficiency of cathepsin D | Inferred relationship | Some | 1 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set