Nephrogenic diabetes insipidus: A rare inherited condition where the kidneys can't concentrate the urine sufficiently which results in excessive urination and thirst. The condition occurs because the kidneys are unable to respond to the antidiuretic hormone. More detailed information about the symptoms, causes, and treatments of Nephrogenic diabetes insipidus is available below.
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See full list of 22 causes of Nephrogenic diabetes insipidus
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Types of Nephrogenic diabetes insipidus
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A polyuric disorder characterized by normal rates of renal filtration and solute excretion, but a persistent hypotonic urine. This condition is due to the failure of renal tubules to respond to antidiuretic hormones, such as vasopressin, to reduce urine volume. Tubular insensitivity to vasopressin can result from genetic defects, diseases, drug effects, or may occur with pregnancy. - (Source - Diseases Database)
Diabetes insipidus caused by a failure of the kidney to respond to normal levels of vasopressin - (Source - WordNet 2.1)
Nephrogenic diabetes insipidus is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Nephrogenic diabetes insipidus, or a subtype of Nephrogenic diabetes insipidus,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Nephrogenic diabetes insipidus as a "rare disease".
Source - Orphanet
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