impaired renal function disease diabetes insipidus inherited renal tubular disease nephrogenic diabetes insipidus ADH resistant diabetes insipidus COHD:438476 DOID:12387 GARD:0007178 ICD10:N25.1 ICD9:588.1 MESH:D018500 MONDO:0016383 MedDRA:10029147 NCIT:C84919 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. Orphanet:223 SCTID:111395007 UMLS:C0162283 diabetes insipidus nephrogenic diabetes insipidus nephrogenic X-linked diabetes insipidus nephrogenic type 1 vasopressin-resistant diabetes insipidus rare renal tubular disease