Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3657381018 | Severe combined immunodeficiency due to complete RAG1 (recombination activating gene 1) and/or RAG2 (recombination activating gene 2) deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3657382013 | SCID (severe combined immunodeficiency) due to complete RAG1/2 deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3657384014 | Severe combined immunodeficiency due to complete RAG1 and/or RAG2 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3657386011 | Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3657387019 | Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency | Finding site | Structure of immune system | true | Inferred relationship | Existential restriction modifier | 1 | |
Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency | Is a | Severe combined immunodeficiency with low T- and B-cell numbers | true | Inferred relationship | Existential restriction modifier | ||
Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency | Pathological process | Abnormal immune process | true | Inferred relationship | Existential restriction modifier | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets