Related MeSH Hierarchy (4)
Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Kidney Diseases » Diabetes Insipidus » Diabetes Insipidus, Neurogenic
Diseases [C] » Urogenital Diseases [C12] » Female Urogenital Diseases and Pregnancy Complications » Female Urogenital Diseases » Urologic Diseases » Kidney Diseases » Diabetes Insipidus » Diabetes Insipidus, Neurogenic
Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urologic Diseases » Kidney Diseases » Diabetes Insipidus » Diabetes Insipidus, Neurogenic
Diseases [C] » Endocrine System Diseases [C19] » Pituitary Diseases » Diabetes Insipidus » Diabetes Insipidus, Neurogenic
Description
A genetic or acquired polyuric disorder caused by a deficiency of VASOPRESSINS secreted by the NEUROHYPOPHYSIS. Clinical signs include the excretion of large volumes of dilute URINE; HYPERNATREMIA; THIRST; and polydipsia. Etiologies include HEAD TRAUMA; surgeries and diseases involving the HYPOTHALAMUS and the PITUITARY GLAND. This disorder may also be caused by mutations of genes such as ARVP encoding vasopressin and its corresponding neurophysin (NEUROPHYSINS). MeSH
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Approved Indicated Drugs (1)
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Other Experimental Indicated Drugs (2)
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