Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 119475016 | SCID due to absent class II HLA antigens | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 119476015 | Bare lymphocyte syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 501993010 | BLS - Bare lymphocyte syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 812122018 | SCID due to absent class II HLA antigens (disorder) | en | Fully specified name | Inactive | Entire term case sensitive | SNOMED CT core module |
| 2612641010 | Severe combined immunodeficiency (SCID) due to absent class II HLA antigens (disorder) | en | Fully specified name | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 2621192017 | Severe combined immunodeficiency (SCID) due to absent class II HLA antigens | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 2914021019 | Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 2914447015 | Severe combined immunodeficiency due to absent class II human leukocyte antigens | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Severe combined immunodeficiency due to absent class II human leukocyte antigens | Is a | Severe combined immunodeficiency disease | true | Inferred relationship | Existential restriction modifier | ||
| Severe combined immunodeficiency due to absent class II human leukocyte antigens | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
| Severe combined immunodeficiency due to absent class II human leukocyte antigens | Severity | Severe | false | Inferred relationship | Existential restriction modifier | ||
| Severe combined immunodeficiency due to absent class II human leukocyte antigens | Finding site | Lymphocyte | false | Inferred relationship | Existential restriction modifier | ||
| Severe combined immunodeficiency due to absent class II human leukocyte antigens | Finding site | Structure of immune system | false | Inferred relationship | Existential restriction modifier | ||
| Severe combined immunodeficiency due to absent class II human leukocyte antigens | Is a | Disorder of immune structure | false | Inferred relationship | Existential restriction modifier | ||
| Severe combined immunodeficiency due to absent class II human leukocyte antigens | Has definitional manifestation | Immune system finding | false | Inferred relationship | Existential restriction modifier | ||
| Severe combined immunodeficiency due to absent class II human leukocyte antigens | Finding site | Body system structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Severe combined immunodeficiency due to absent class II human leukocyte antigens | Pathological process | Abnormal immune process | true | Inferred relationship | Existential restriction modifier | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR