Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
356777011 | Severe deficiency of arylsulfatase | en | Synonym | Active | Case insensitive | SNOMED CT core |
356778018 | Severe deficiency of arylsulphatase | en | Synonym | Active | Case insensitive | SNOMED CT core |
356779014 | Arylsulfatase A deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
356780012 | Cerebroside sulphatase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
356781011 | ARSA - Arylsulphatase A deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
356782016 | ARSA - Arylsulfatase A deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
356783014 | Cerebroside sulfatase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
356784015 | Arylsulphatase A deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
626853018 | Arylsulfatase A deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Arylsulfatase A deficiency | Is a | Metachromatic leukodystrophy | true | Inferred relationship | Some | ||
Arylsulfatase A deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
Arylsulfatase A deficiency | Occurrence | Congenital | false | Inferred relationship | Some | ||
Arylsulfatase A deficiency | Is a | Metachromatic leukodystrophy | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Metachromatic leucodystrophy, adult type | Is a | False | Arylsulfatase A deficiency | Inferred relationship | Some | |
Metachromatic leucodystrophy, juvenile type | Is a | False | Arylsulfatase A deficiency | Inferred relationship | Some | |
Metachromatic leucodystrophy, late infantile type | Is a | False | Arylsulfatase A deficiency | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set