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expanddiabetes insipidus (MONDO:0004782)
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expandimpaired renal function disease (MONDO:0001343)
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expandinherited renal tubular disease (MONDO:0015962)
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expandrare renal tubular disease (MONDO:0019744)
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..expandnephrogenic diabetes insipidus ()

       Child Nodes:
........expanddiabetes insipidus, nephrogenic, autosomal ()
........expanddiabetes insipidus, nephrogenic, X-linked ()



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..expandhyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome ()
..expandhypotonia-cystinuria syndrome type 1 ()
..expandidiopathic inherited hypercalciuria ()
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..expandJeune syndrome ()
..expandmitochondrial DNA depletion syndrome, hepatocerebrorenal form ()
..expandnephrogenic diabetes insipidus ()
..expandnephrogenic diabetes insipidus-intracranial calcification syndrome ()
..expandnephrogenic syndrome of inappropriate antidiuresis ()
..expandnephronophthisis (disease) ()
..expandoculocerebrorenal syndrome ()
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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:16383
Name:nephrogenic diabetes insipidus
Definition: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 litres in children.
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Synonyms:ADH resistant diabetes insipidus; diabetes insipidus nephrogenic; diabetes insipidus nephrogenic type 1; diabetes insipidus nephrogenic X-linked; vasopressin-resistant diabetes insipidus
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Reference: MedGen:
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