A genetic or acquired polyuric disorder characterized by persistent hypotonic urine and HYPOKALEMIA. This condition is due to renal tubular insensitivity to VASOPRESSIN and failure to reduce urine volume. It may be the result of mutations of genes encoding VASOPRESSIN RECEPTORS or aquaporin-2 (AQUAPORINS); KIDNEY DISEASES; adverse drug effects; or complications from PREGNANCY.
Also Known As:
Diabetes Insipidus, Nephrogenic; Acquired Nephrogenic Diabetes Insipidus; Congenital Nephrogenic Diabetes Insipidus; Diabetes Insipidus, Nephrogenic, Type I; Diabetes Insipidus, Nephrogenic, Type II; Nephrogenic Diabetes Insipidus, Type I; Nephrogenic Diabetes Insipidus, Type II