Status: current, Primitive. Date: 30-Nov 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4669941019 | Behçet-like disease due to HA20 | en | Synonym | Active | Case sensitive | SNOMED CT core |
4669942014 | Hereditary paediatric Behçet-like disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4669943016 | Hereditary pediatric Behçet-like disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4669944010 | Hereditary pediatric Behçet-like disease (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
4669945011 | Behçet-like disease due to haploinsufficiency of A20 | en | Synonym | Active | Case sensitive | SNOMED CT core |
4669946012 | A rare autosomal dominant autoinflammatory syndrome characterized by early onset systemic inflammation with autoimmune manifestations and more rarely, humoral immune deficiency and increased production of circulating proinflammatory cytokines. Variable manifestations include recurrent oral aphthous ulcers, genital ulcers, arthralgia or arthritis, periodic fever, uveitis and severe gastrointestinal involvement (pain, diarrhea, vomiting, rectal bleeding). | en | Definition | Active | Case sensitive | SNOMED CT core |
4669947015 | A rare autosomal dominant autoinflammatory syndrome characterised by early onset systemic inflammation with autoimmune manifestations and more rarely, humoral immune deficiency and increased production of circulating proinflammatory cytokines. Variable manifestations include recurrent oral aphthous ulcers, genital ulcers, arthralgia or arthritis, periodic fever, uveitis and severe gastrointestinal involvement (pain, diarrhoea, vomiting, rectal bleeding). | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary paediatric Behçet-like disease | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Hereditary paediatric Behçet-like disease | Is a | Inflammatory disorder | true | Inferred relationship | Some | ||
Hereditary paediatric Behçet-like disease | Is a | Systemic disease | true | Inferred relationship | Some | ||
Hereditary paediatric Behçet-like disease | Is a | Recurrent disease | true | Inferred relationship | Some | ||
Hereditary paediatric Behçet-like disease | Clinical course | Recurrent | true | Inferred relationship | Some | 3 | |
Hereditary paediatric Behçet-like disease | Associated morphology | Inflammatory morphology | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set