Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
diabète insipide néphrogénique héréditaire | Is a | False | Arginine vasopressin resistance (disorder) | Inferred relationship | Some | |
Acquired vasopressin resistance | Is a | True | Arginine vasopressin resistance (disorder) | Inferred relationship | Some | |
Partial vasopressin resistance | Is a | True | Arginine vasopressin resistance (disorder) | Inferred relationship | Some | |
A rare, genetic, renal tubular disease characterized by nephrogenic diabetes insipidus, intracerebral calcifications, intellectual disability, short stature and facial dysmorphism. There have been no further descriptions in the literature since 1990. | Is a | True | Arginine vasopressin resistance (disorder) | Inferred relationship | Some | |
Hereditary vasopressin resistance | Is a | True | Arginine vasopressin resistance (disorder) | Inferred relationship | Some | |
Secondary arginine vasopressin resistance (disorder) | Is a | True | Arginine vasopressin resistance (disorder) | Inferred relationship | Some |
This concept is not in any reference sets