Status: retired, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2463751015 | Alkaptonuria (finding) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 476131011 | Alkaptonuria | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Alkaptonuria | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
| Alkaptonuria | Is a | Aciduria | false | Inferred relationship | Some | ||
| Alkaptonuria | Finding site | Urinary system structure | false | Inferred relationship | Some | ||
| Alkaptonuria | Interprets | Contents of urine | false | Inferred relationship | Some | ||
| Alkaptonuria | Due to | Homogentisate 1,2-dioxygenase deficiency | false | Inferred relationship | Some | 1 | |
| Alkaptonuria | Interprets | Evaluation of urine specimen | false | Inferred relationship | Some | 2 | |
| Alkaptonuria | Interprets | Urine observable | false | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Ochronosis due to alkaptonuria | Associated etiologic finding | False | Alkaptonuria | Inferred relationship | Some |
Reference Sets
Australian dialect reference set
Concept inactivation indicator reference set
Description inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set
FHIR