Diabetes Insipidus, Neurohypophyseal Type

Alternative Names

  • Diabetes Insipidus, Primary Central
  • CDI
  • Diabetes Insipidus, Cranial Type

Associated Genes

Arginine Vasopressin
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WHO-ICD-10 version:2010

Diseases of the genitourinary system

Other disorders of kidney and ureter

OMIM Number

125700

Mode of Inheritance

Autosomal dominant

Gene Map Locus

20p13

Description

Neurohypophyseal diabetes insipidus is an autosomal dominant disorder of free water conservation characterized by childhood onset of polyuria and polydipsia. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
125700.1.1LebanonMaleNoNo Polyuria; PolydipsiaNM_000490.5:c.20C>T, NM_000490.5:c.121-2A>GHeterozygousAutosomal, RecessiveBourdet et al, 2016 Patient born to a Le...
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