Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Feb 2024. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5287782012 | X-linked hereditary vasopressin resistance | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5287783019 | X-linked hereditary arginine vasopressin resistance (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5289669019 | X-linked hereditary arginine vasopressin resistance | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5289670018 | X-linked hereditary AVP-R (arginine vasopressin resistance) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| X-linked hereditary vasopressin resistance | Is a | X-linked hereditary disease | true | Inferred relationship | Some | ||
| X-linked hereditary vasopressin resistance | Is a | Hereditary vasopressin resistance | true | Inferred relationship | Some | ||
| X-linked hereditary vasopressin resistance | Finding site | Urinary system structure (body structure) | true | Inferred relationship | Some | 2 | |
| X-linked hereditary vasopressin resistance | Interprets | Urine output observable | true | Inferred relationship | Some | 1 | |
| X-linked hereditary vasopressin resistance | Has interpretation | Increased | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome (disorder) | Is a | True | X-linked hereditary vasopressin resistance | Inferred relationship | Some |
This concept is not in any reference sets
FHIR