Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2971858017 | Mucopolysaccharidosis type VII (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
493710017 | Sly disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
493711018 | Mucopolysaccharidosis type VII | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
493712013 | Beta-glucuronidase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
493713015 | MPS VII - Mucopolysaccharidosis VII | en | Synonym | Active | Case sensitive | SNOMED CT core |
73228011 | Mucopolysaccharidosis, MPS-VII | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
73229015 | Sly syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
73230013 | beta-Glucuronidase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
73231012 | GUSB deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
73232017 | GUS deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Mucopolysaccharidosis, MPS-VII | Is a | Mucopolysaccharidosis | true | Inferred relationship | Some | ||
Mucopolysaccharidosis, MPS-VII | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Mucopolysaccharidosis, MPS-VII | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Mucopolysaccharidosis, MPS-VII | Finding site | Body system structure | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set