Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4667435014 | CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| 4667436010 | CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 4667437018 | CAIN (CEBPE-associated autoinflammation, immunodeficiency, neutrophil dysfunction) syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 4667438011 | CEBPE-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Is a | Hereditary periodic fever | true | Inferred relationship | Existential restriction modifier | ||
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Is a | Chronic disease of immune function | false | Inferred relationship | Existential restriction modifier | ||
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Is a | Primary immune deficiency disorder | true | Inferred relationship | Existential restriction modifier | ||
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Clinical course | Recurrent | true | Inferred relationship | Existential restriction modifier | 2 | |
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Associated with | Fever | true | Inferred relationship | Existential restriction modifier | 3 | |
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Associated morphology | Inflammatory morphology | true | Inferred relationship | Existential restriction modifier | 1 | |
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Pathological process | Abnormal immune process | true | Inferred relationship | Existential restriction modifier | 1 | |
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Interprets | Body temperature | true | Inferred relationship | Existential restriction modifier | 4 | |
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Has interpretation | Above reference range | true | Inferred relationship | Existential restriction modifier | 4 | |
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Is a | Hereditary disorder of immune system | true | Inferred relationship | Existential restriction modifier | ||
| CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome | Finding site | Structure of immune system | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR