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 |
5287792016 | Hereditary arginine vasopressin-related polyuria (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5287793014 | Hereditary arginine vasopressin-related polyuria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5289639014 | Hereditary vasopressin-related polyuria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5289646017 | Hereditary AVP (arginine vasopressin)-related polyuria | 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 |
Hereditary arginine vasopressin-related polyuria (disorder) | Is a | Arginine vasopressin-related polyuria (disorder) | true | Inferred relationship | Some | ||
Hereditary arginine vasopressin-related polyuria (disorder) | Is a | Hereditary disease | true | Inferred relationship | Some | ||
Hereditary arginine vasopressin-related polyuria (disorder) | Interprets | Urine output observable | true | Inferred relationship | Some | 1 | |
Hereditary arginine vasopressin-related polyuria (disorder) | Has interpretation | Increased | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hereditary vasopressin resistance | Is a | True | Hereditary arginine vasopressin-related polyuria (disorder) | Inferred relationship | Some | |
Autosomal dominant hereditary arginine vasopressin deficiency (disorder) | Is a | True | Hereditary arginine vasopressin-related polyuria (disorder) | Inferred relationship | Some | |
Autosomal recessive hereditary arginine vasopressin deficiency (disorder) | Is a | True | Hereditary arginine vasopressin-related polyuria (disorder) | Inferred relationship | Some |
This concept is not in any reference sets