Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Nov 2024. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5406581012 | Autosomal dominant combined immunodeficiency due to ERBIN deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5406582017 | Autosomal dominant combined immunodeficiency due to erbb2 interacting protein deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5406583010 | Autosomal dominant combined immunodeficiency due to erbb2 interacting protein deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5406619011 | Autosomal dominant hyperimmunoglobulin E syndrome due to ERBIN deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5406620017 | Autosomal dominant hyperimmunoglobulin E syndrome due to ERBB2IP defect | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant combined immunodeficiency due to ERBIN deficiency | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Autosomal dominant combined immunodeficiency due to ERBIN deficiency | Is a | Hyperimmunoglobulin E syndrome | true | Inferred relationship | Some | ||
| Autosomal dominant combined immunodeficiency due to ERBIN deficiency | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 1 | |
| Autosomal dominant combined immunodeficiency due to ERBIN deficiency | Interprets | Immunoglobulin E measurement | true | Inferred relationship | Some | 2 | |
| Autosomal dominant combined immunodeficiency due to ERBIN deficiency | Has interpretation | Above reference range | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
FHIR