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 |
356246010 | Familial central diabetes insipidus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5287681011 | Familial vasopressin deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5287682016 | Familial arginine vasopressin deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5289636019 | Familial AVP-D (arginine vasopressin deficiency) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5289637011 | Familial arginine vasopressin deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial vasopressin deficiency | Is a | Vasopressin deficiency | true | Inferred relationship | Some | ||
Familial vasopressin deficiency | Is a | Familial vasopressin-related polyuria | true | Inferred relationship | Some | ||
Familial vasopressin deficiency | Finding site | Pars nervosa of pituitary gland | false | Inferred relationship | Some | ||
Familial vasopressin deficiency | Finding site | Entire endocrine gonad (body structure) | false | Inferred relationship | Some | ||
Familial vasopressin deficiency | Interprets | Nutritional deficiency (finding) | false | Inferred relationship | Some | ||
Familial vasopressin deficiency | Finding site | Neurohypophysis structure | true | Inferred relationship | Some | 1 | |
Familial vasopressin deficiency | Interprets | Urine output observable | true | Inferred relationship | Some | 2 | |
Familial vasopressin deficiency | Has interpretation | Increased | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Autosomal dominant hereditary arginine vasopressin deficiency (disorder) | Is a | True | Familial vasopressin deficiency | Inferred relationship | Some | |
Autosomal recessive hereditary arginine vasopressin deficiency (disorder) | Is a | True | Familial vasopressin deficiency | Inferred relationship | Some |
This concept is not in any reference sets