Nephrogenic Diabetes Insipidus

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; KIDNEY DISEASES; adverse drug effects; or complications from PREGNANCY.

Also Known As:

Diabetes Insipidus, Nephrogenic; ADH-Resistant Diabetes Insipidus; Acquired Nephrogenic Diabetes Insipidus; Congenital Nephrogenic Diabetes Insipidus; Diabetes Insipidus Renalis; Diabetes Insipidus, Nephrogenic, Autosomal; Diabetes Insipidus, Nephrogenic, Type 1; Diabetes Insipidus, Nephrogenic, Type I; Diabetes Insipidus, Nephrogenic, Type II; Diabetes Insipidus, Nephrogenic, X-Linked; Nephrogenic Diabetes Insipidus, Type I; Nephrogenic Diabetes Insipidus, Type II; Vasopressin-Resistant Diabetes Insipidus

Urogenital Diseases: 126
- Urologic Diseases: 799
  - Kidney Diseases: 12250
    - Diabetes Insipidus: 2556
      - Nephrogenic Diabetes Insipidus: 977
- Female Urogenital Diseases and Pregnancy Complications
  - Female Urogenital Diseases
    - Urologic Diseases: 799
      - Kidney Diseases: 12250
        Diabetes Insipidus: 2556
        Nephrogenic Diabetes Insipidus: 977
- Male Urogenital Diseases
  - Urologic Diseases: 799
    - Kidney Diseases: 12250
      - Diabetes Insipidus: 2556
        Nephrogenic Diabetes Insipidus: 977

Nadine Kümmerer Selected Research

Nadine Kümmerer Research Topics

Disease

Drug/Important Bio-Agent (IBA)