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 |
| 3424323018 | Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3424324012 | Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3424325013 | Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3424326014 | Mendelian susceptibility to mycobacterial disease due to complete ISG15 (interferon stimulated gene 15) deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5403030018 | Mendelian susceptibility to mycobacterial diseases (MSMD) due to complete ISG15 deficiency is a genetic variant of MSMD characterized by Bacille Calmette-Guérin (BCG) infections. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5403031019 | Mendelian susceptibility to mycobacterial diseases (MSMD) due to complete ISG15 deficiency is a genetic variant of MSMD characterised by Bacille Calmette-Guérin (BCG) infections. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Due to | Chromosomal disorder (disorder) | false | Inferred relationship | Some | 1 | |
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Is a | Immunodeficiency associated with chromosomal abnormality | false | Inferred relationship | Some | ||
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | false | Inferred relationship | Some | 2 | |
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Is a | Mendelian susceptibility to mycobacterial disease | true | Inferred relationship | Some | ||
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Is a | Type I interferonopathy | true | Inferred relationship | Some | ||
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Is a | Hereditary disorder of immune system | true | Inferred relationship | Some | ||
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Is a | Autoimmune disease | true | Inferred relationship | Some | ||
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Finding site | Structure of immune system (body structure) | true | Inferred relationship | Some | 1 | |
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR