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 |
| 139496018 | Iminoglycinuria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 139497010 | Iminoglycinuria, NOS | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 474901000241114 | iminoglycinurie (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 825899010 | Iminoglycinuria (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 925651000172111 | iminoglycinurie | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Iminoglycinuria | est un(e) (attribut) | maladie métabolique du rein | true | Inferred relationship | Some | ||
| Iminoglycinuria | est un(e) (attribut) | Congenital anomaly of trunk | false | Inferred relationship | Some | ||
| Iminoglycinuria | est un(e) (attribut) | Specific renal tubule transport defect | true | Inferred relationship | Some | ||
| Iminoglycinuria | est un(e) (attribut) | Amino acid transport disorder | true | Inferred relationship | Some | ||
| Iminoglycinuria | est un(e) (attribut) | Hereditary disorder of the urinary system | false | Inferred relationship | Some | ||
| Iminoglycinuria | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Iminoglycinuria | localisation d'une constatation (attribut) | structure d'un rein | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Neonatal iminoglycinuria | est un(e) (attribut) | True | Iminoglycinuria | Inferred relationship | Some | |
| iminoglycinurie rénale familiale | est un(e) (attribut) | True | Iminoglycinuria | Inferred relationship | Some |
This concept is not in any reference sets
FHIR