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Nephrogenic diabetes insipidus

rare

Nephrogenic diabetes insipidus (NDI) is characterized by polyuria with polydipsia, recurrent bouts of fever, constipation, and acute hypernatremic dehydration after birth that may cause neurological sequelae. Polyuria may exceed 10 liters in children.

Identifiers
MONDO:0016383 Orphanet:223
Part of
Diabetes insipidusImpaired renal function diseaseInherited renal tubular disease
Also known as
ADH resistant diabetes insipidus · diabetes insipidus nephrogenic · diabetes insipidus nephrogenic type 1 · diabetes insipidus nephrogenic X-linked

Subtypes

All diseases Rare only

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