Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 129952019 | Histidine transport defect | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 129953012 | Hyperhistidinuria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 129954018 | Histidinuria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 129955017 | Renal histidinuria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 819238016 | Histidine transport defect (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Histidine transport defect | est un(e) (attribut) | maladie métabolique du rein | true | Inferred relationship | Some | ||
| Histidine transport defect | est un(e) (attribut) | Congenital anomaly of trunk | false | Inferred relationship | Some | ||
| Histidine transport defect | est un(e) (attribut) | trouble du métabolisme de l'histidine (trouble) | true | Inferred relationship | Some | ||
| Histidine transport defect | est un(e) (attribut) | Hereditary disorder of the urinary system | false | Inferred relationship | Some | ||
| Histidine transport defect | est un(e) (attribut) | Amino acid transport disorder | true | Inferred relationship | Some | ||
| Histidine transport defect | est un(e) (attribut) | Specific renal tubule transport defect | true | Inferred relationship | Some | ||
| Histidine transport defect | localisation d'une constatation (attribut) | structure d'un rein | true | Inferred relationship | Some | 1 | |
| Histidine transport defect | survenue (attribut) | congénital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR