Neurohypophyseal diabetes insipidus

Hereditary central diabetes insipidus is a rare genetic subtype of central diabetes insipidus (CDI) characterized by polyuria and polydipsia due to a deficiency in vasopressin (AVP) synthesis.

Also known as: ADH deficiency, AVP deficiency, Arginine vasopressin deficiency, antidiuretic hormone deficiency, diabetes insipidus of pituitary gland, hereditary CDI, hereditary neurogenic diabetes insipidus, pituitary gland diabetes insipidus

11 clinical trials for this condition and its sub-types.