Status: current, Primitive. Date: 31-Jul 2004. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2465493015 | Ochronosis due to homogentisate 1,2-dioxygenase deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
2471769016 | Alcaptonuric ochronosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
2477705016 | Pigmentation due to alkaptonuria | en | Synonym | Active | Case insensitive | SNOMED CT core |
2477706015 | Ochronosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
2477707012 | Alkaptonuric ochronosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
2477708019 | Ochronosis due to homogentisate 1,2-dioxygenase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
2477709010 | Ochronosis due to alkaptonuria | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Alcaptonuric ochronosis | Is a | Skin deposits | true | Inferred relationship | Some | ||
Alcaptonuric ochronosis | Is a | Disorder of skin pigmentation | true | Inferred relationship | Some | ||
Alcaptonuric ochronosis | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
Alcaptonuric ochronosis | Is a | Degenerative disorder | false | Inferred relationship | Some | ||
Alcaptonuric ochronosis | Associated morphology | Pigment deposition | true | Inferred relationship | Some | 1 | |
Alcaptonuric ochronosis | Due to | Homogentisate 1,2-dioxygenase deficiency | true | Inferred relationship | Some | 2 | |
Alcaptonuric ochronosis | Associated morphology | Degeneration | false | Inferred relationship | Some | ||
Alcaptonuric ochronosis | Is a | Disorder of pigmentation | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set