Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3330457013 | Severe combined immunodeficiency with hypereosinophilia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3330458015 | Severe combined immunodeficiency with hypereosinophilia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3330459011 | Omenn syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402817013 | Omenn syndrome (OS) is an inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402818015 | Omenn syndrome (OS) is an inflammatory condition characterised by erythroderma, desquamation, alopecia, chronic diarrhoea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Severe combined immunodeficiency with hypereosinophilia (disorder) | Is a | Severe combined immunodeficiency with low T- and B-cell numbers | true | Inferred relationship | Some | ||
Severe combined immunodeficiency with hypereosinophilia (disorder) | Is a | Hereditary eosinophilia | true | Inferred relationship | Some | ||
Severe combined immunodeficiency with hypereosinophilia (disorder) | Is a | Autosomal recessive severe combined immunodeficiency disease (disorder) | true | Inferred relationship | Some | ||
Severe combined immunodeficiency with hypereosinophilia (disorder) | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
Severe combined immunodeficiency with hypereosinophilia (disorder) | Has definitional manifestation | Eosinophil count above reference range (finding) | false | Inferred relationship | Some | ||
Severe combined immunodeficiency with hypereosinophilia (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Severe combined immunodeficiency with hypereosinophilia (disorder) | Finding site | Structure of immune system (body structure) | true | Inferred relationship | Some | 3 | |
Severe combined immunodeficiency with hypereosinophilia (disorder) | Has interpretation | Above reference range | true | Inferred relationship | Some | 1 | |
Severe combined immunodeficiency with hypereosinophilia (disorder) | Interprets | Eosinophil count | true | Inferred relationship | Some | 1 | |
Severe combined immunodeficiency with hypereosinophilia (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 2 | |
Severe combined immunodeficiency with hypereosinophilia (disorder) | Is a | Disorder of eosinophil (disorder) | true | Inferred relationship | Some | ||
Severe combined immunodeficiency with hypereosinophilia (disorder) | Finding site | Eosinophilic granulocytic cell | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)