Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 486812010 | Disorder of proline and hydroxyproline metabolism | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 63061012 | Disorder of proline AND/OR hydroxyproline metabolism | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 769708013 | Disorder of proline AND/OR hydroxyproline metabolism (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder of proline AND/OR hydroxyproline metabolism | Is a | Disorder of amino acid metabolism | false | Inferred relationship | Some | ||
| Disorder of proline AND/OR hydroxyproline metabolism | Is a | Disorder of amino acid and organic acid metabolism | true | Inferred relationship | Some | ||
| Disorder of proline AND/OR hydroxyproline metabolism | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Disorder of proline AND/OR hydroxyproline metabolism | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Autosomal recessive cutis laxa type 2B | Is a | True | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some | |
| Cutis laxa-corneal clouding-oligophrenia syndrome | Is a | True | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some | |
| Deficiency of pyrroline-2-carboxylate reductase | Is a | True | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some | |
| Deficiency of pyrroline-5-carboxylate reductase | Is a | True | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some | |
| Pipecolic acidaemia | Is a | True | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some | |
| Hyperhydroxyprolinaemia | Is a | True | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some | |
| Prolinuria | Is a | True | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some | |
| Hyperprolinaemia | Is a | True | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some | |
| Deficiency of proline dipeptidase | Is a | True | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some | |
| Proline dipeptidase deficiency | Is a | False | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some | |
| Hyperprolinaemia | Is a | False | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some | |
| Iminoacidopathy | Is a | True | Disorder of proline AND/OR hydroxyproline metabolism | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR