Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-May 2022. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5048484011 | Tripeptidyl-peptidase II deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
5048485012 | TRIANGLE (TPPII-related immunodeficiency, autoimmunity, neurodevelopmental delay, impaired glycolysis, lysosomal expansion) disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
5048486013 | TPPII-related immunodeficiency, autoimmunity and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
5048487016 | Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
5048488014 | Autoimmune haemolytic anaemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
5048489018 | TPPII (tripeptidyl-peptidase II) deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
5048490010 | Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
5048491014 | Evans syndrome associated with primary immunodeficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome | Is a | Combined immunodeficiency disease | true | Inferred relationship | Existential restriction modifier | ||
Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome | Pathological process | Autoimmune process | true | Inferred relationship | Existential restriction modifier | 1 | |
Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome | Is a | Autoimmune disease | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets