Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2015. Module: SNOMED CT Sweden NRC maintained module (core metadata concept)
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3744881000052110 | Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) (procedure) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| 3744891000052112 | Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| 3744901000052113 | enzymersättningsbehandling vid Pompes sjukdom | sv | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) (procedure) | Is a | åtgärd med fokus på specifikt kliniskt fynd | false | Inferred relationship | Some | ||
| Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) (procedure) | Is a | Drug therapy (procedure) | true | Inferred relationship | Some | ||
| Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) (procedure) | Has focus | brist på lysosomal alfa-1,4-glukosidas, infantil debut | false | Inferred relationship | Some | ||
| Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) (procedure) | Direct substance | enzymläkemedel | false | Inferred relationship | Some | 3 | |
| Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) (procedure) | Has intent | Therapeutic | true | Inferred relationship | Some | 4 | |
| Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) (procedure) | Method | Administration - action | true | Inferred relationship | Some | 1 | |
| Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) (procedure) | Direct substance | Drug or medicament (substance) | true | Inferred relationship | Some | 1 | |
| Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) (procedure) | Has focus | Glycogen storage disease due to acid maltase deficiency | true | Inferred relationship | Some | 2 | |
| Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) (procedure) | Direct substance | Enzyme | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR