Disease ID | Source | Name | Description |
125800 | OMIM | Diabetes insipidus, nephrogenic, autosomal (ANDI) | A disorder caused by the inability of the renal collecting ducts to absorb water in response to arginine vasopressin. Characterized by excessive water drinking (polydipsia), excessive urine excretion (polyuria), persistent hypotonic urine, and hypokalemia. Inheritance can be autosomal dominant or recessive. The disease is caused by variants affecting the gene represented in this entry. |