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 |
| 1234522018 | Neutral amino acid transport defect | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 134190018 | Neutral 1 amino acid transport defect | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 134191019 | Hartnup disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 134192014 | Hartnup disorder | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 822114012 | Neutral 1 amino acid 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 |
| Neutral 1 amino acid transport defect | est un(e) (attribut) | maladie métabolique du rein | true | Inferred relationship | Some | ||
| Neutral 1 amino acid transport defect | est un(e) (attribut) | Congenital anomaly of trunk | false | Inferred relationship | Some | ||
| Neutral 1 amino acid transport defect | est un(e) (attribut) | Specific renal tubule transport defect | true | Inferred relationship | Some | ||
| Neutral 1 amino acid transport defect | est un(e) (attribut) | Hereditary disorder of the urinary system | false | Inferred relationship | Some | ||
| Neutral 1 amino acid transport defect | est un(e) (attribut) | Amino acid transport disorder | true | Inferred relationship | Some | ||
| Neutral 1 amino acid transport defect | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Neutral 1 amino acid transport defect | localisation d'une constatation (attribut) | structure d'un rein | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hartnup disorder, renal type | est un(e) (attribut) | True | Neutral 1 amino acid transport defect | Inferred relationship | Some | |
| Hartnup disorder, renal/jejunal type | est un(e) (attribut) | True | Neutral 1 amino acid transport defect | Inferred relationship | Some |
Reference Sets
Description inactivation indicator reference set
FHIR