Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1782840016 | Autosomal recessive hyper-IgM syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 2968614012 | Autosomal recessive hyper- immunoglobulin M syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3424904019 | Autosomal recessive hyperimmunoglobulin M syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3424905018 | Autosomal recessive hyperimmunoglobulin M syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive hyperimmunoglobulin M syndrome | Is a | Hyperimmunoglobulin M syndrome | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive hyperimmunoglobulin M syndrome | Finding site | Structure of immune system | false | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive hyperimmunoglobulin M syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive hyperimmunoglobulin M syndrome | Has definitional manifestation | Immune system finding | false | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive hyperimmunoglobulin M syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive hyperimmunoglobulin M syndrome | 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
FHIR