Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3439277014 | Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3439278016 | Immunodeficiency by defective expression of human leukocyte antigen class 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3439279012 | Bare lymphocyte syndrome type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3439280010 | Bare lymphocyte syndrome type I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3439281014 | Immunodeficiency by defective expression of HLA (human leukocyte antigen) class 1 | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3439282019 | Immunodeficiency by defective expression of human leukocyte antigen class I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3439283012 | A very rare, primary genetic immunodeficiency disorder with characteristic of partial or complete absence of human leukocyte antigen class I expression resulting in a non-specific clinical picture of impaired immune response and susceptibility to infections. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder) | Is a | Autosomal recessive severe combined immunodeficiency disease (disorder) | true | Inferred relationship | Some | ||
| Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder) | Finding site | Body system structure | true | Inferred relationship | Some | 2 | |
| Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder) | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR