Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356777011 | Severe deficiency of arylsulfatase | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 356778018 | Severe deficiency of arylsulphatase | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 356779014 | Arylsulfatase A deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 356780012 | Cerebroside sulphatase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 356781011 | ARSA - Arylsulphatase A deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 356782016 | ARSA - Arylsulfatase A deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 356783014 | Cerebroside sulfatase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 356784015 | Arylsulphatase A deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 626853018 | Arylsulfatase A deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Arylsulfatase A deficiency | Is a | Metachromatic leucodystrophy | false | Inferred relationship | Existential restriction modifier | ||
| Arylsulfatase A deficiency | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Arylsulfatase A deficiency | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Arylsulfatase A deficiency | Is a | Metachromatic leucodystrophy | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Metachromatic leukodystrophy, adult type | Is a | False | Arylsulfatase A deficiency | Inferred relationship | Existential restriction modifier | |
| Metachromatic leukodystrophy, juvenile type | Is a | False | Arylsulfatase A deficiency | Inferred relationship | Existential restriction modifier | |
| Metachromatic leukodystrophy, late infantile type | Is a | False | Arylsulfatase A deficiency | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR