Status: current, Primitive. Date: 31-Jul 2015. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3083301019 | Deficiency of phosphomannomutase 2 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3083473016 | Deficiency of phosphomannomutase 2 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Deficiency of phosphomannomutase 2 | Is a | Specific enzyme deficiency | true | Inferred relationship | Some | ||
| Deficiency of phosphomannomutase 2 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital disorder of glycosylation type Ia | Due to | True | Deficiency of phosphomannomutase 2 | Inferred relationship | Some | 1 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR