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 and metabolic disease
Brite
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 other specified disorders of pituitary gland
     H00253  Neurohypophyseal diabetes insipidus
Pathway-based classification of diseases [BR:br08402]
 Endocrine system
  nt06325  Hormone/cytokine signaling
   H00253  Neurohypophyseal diabetes insipidus
Pathway
hsa04962  Vasopressin-regulated water reabsorption
Network
nt06325 Hormone/cytokine 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
PMID:16713494
  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
PMID:12874957
  Authors
Christensen JH, Siggaard C, Rittig S
  Title
Autosomal dominant familial neurohypophyseal diabetes insipidus.
  Journal
APMIS Suppl 92-5 (2003)
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