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Neurohypophyseal diabetes insipidus
Neurohypophyseal diabetes insipidus is an autosomal dominant disorder of free water conservation characterized by childhood onset of polyuria and polydipsia. Affected individuals are apparently normal at birth, but characteristically develop symptoms of vasopressin deficiency during childhood (summary by Wahlstrom et al., 2004). [from OMIM]
Central diabetes insipidus
A form of diabetes insipidus related to a failure of vasopressin (AVP) release from the hypothalamus. [from HPO]
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