Orphanet: Nephrogenic diabetes insipidus
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Nephrogenic diabetes insipidus

Disease definition

A rare, genetic renal tubular disease that is characterized by polyuria with polydipsia, recurrent bouts of fever, constipation, and acute hypernatremic dehydration after birth that may cause neurological sequelae.

ORPHA:223

Classification level: Disorder
  • Synonym(s): -
  • Prevalence: 1-9 / 1 000 000
  • Inheritance: Autosomal dominant or Autosomal recessive or X-linked recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: N25.1
  • OMIM: 125800  304800
  • UMLS: C0162283
  • MeSH: D018500
  • GARD: 7178
  • MedDRA: 10029147

Detailed information

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