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 |
| 5065852019 | Severe combined immunodeficiency due to CORO1A deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 5065853012 | Severe combined immunodeficiency due to coronin 1A deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 5065854018 | Severe combined immunodeficiency due to coronin 1A deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Severe combined immunodeficiency due to coronin 1A deficiency | Is a | Autosomal recessive severe combined immunodeficiency disease | true | Inferred relationship | Existential restriction modifier | ||
| Severe combined immunodeficiency due to coronin 1A deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Severe combined immunodeficiency due to coronin 1A deficiency | Finding site | Body system structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Severe combined immunodeficiency due to coronin 1A deficiency | Pathological process | Abnormal immune process | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR