Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1782840016 | Autosomal recessive hyper-IgM syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2968614012 | Autosomal recessive hyper- immunoglobulin M syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3424904019 | Autosomal recessive hyperimmunoglobulin M syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3424905018 | Autosomal recessive hyperimmunoglobulin M syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive hyperimmunoglobulin M syndrome (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 2 | |
| Autosomal recessive hyperimmunoglobulin M syndrome (disorder) | est un(e) (attribut) | Hyperimmunoglobulin M syndrome | true | Inferred relationship | Some | ||
| Autosomal recessive hyperimmunoglobulin M syndrome (disorder) | localisation d'une constatation (attribut) | structure du système immunitaire | false | Inferred relationship | Some | ||
| Autosomal recessive hyperimmunoglobulin M syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Autosomal recessive hyperimmunoglobulin M syndrome (disorder) | est défini par la manifestation de (attribut) | Immune system finding | false | Inferred relationship | Some | ||
| Autosomal recessive hyperimmunoglobulin M syndrome (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR