KEGG   DISEASE: Neurohypophyseal diabetes insipidus
Entry
H00253                      Disease                                
Name
Neurohypophyseal diabetes insipidus;
Central diabetes insipidus
  Supergrp
Disorders of antidiuretic hormone (ADH) secretion [DS:H01683]
Description
Neurohypophyseal diabetes insipidus (NDI), also known as central diabetes insipidus, is a heterogeneous condition characterized by polyuria and polydipsia caused by defect of antidiuretic hormone secreted from the pituitary gland.
Category
Endocrine disease; Kidney disease
Brite
Human diseases [BR:br08402]
 Endocrine and metabolic diseases
  Hypothalamus and pituitary gland diseases
   H00253  Neurohypophyseal diabetes insipidus
Human diseases in ICD-11 classification [BR:br08403]
 05 Endocrine, nutritional or metabolic diseases
  Endocrine diseases
   Disorders of the pituitary hormone system
    5A61  Hypofunction or certain specified disorders of pituitary gland
     H00253  Neurohypophyseal diabetes insipidus
Related
pathway
hsa04962  Vasopressin-regulated water reabsorption
Network
nt06326  AVP signaling
Gene
AVP [HSA:551] [KO:K05242]
Drug
Desmopressin acetate [DR:D02235]
Other DBs
ICD-11: 5A61.5
ICD-10: E23.2
MeSH: D020790
OMIM: 125700
Reference
  Authors
Christensen JH, Rittig S
  Title
Familial neurohypophyseal diabetes insipidus--an update.
  Journal
Semin Nephrol 26:209-23 (2006)
DOI:10.1016/j.semnephrol.2006.03.003
Reference
  Authors
Christensen JH, Siggaard C, Rittig S
  Title
Autosomal dominant familial neurohypophyseal diabetes insipidus.
  Journal
APMIS Suppl 92-5 (2003)
LinkDB

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