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Ontology Browser

Term:
neurohypophyseal diabetes insipidus (DOID:12388)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (0) Bonobo: (1) Dog: (1) Squirrel: (0) Pig: (1)
Parent Terms Term With Siblings Child Terms
diabetes insipidus +     
pancreas disease +     
annular pancreas  
cystic fibrosis +   
Dipsogenic Diabetes Insipidus 
endocrine pancreas disease +   
exocrine pancreatic insufficiency +   
Gestational Diabetes Insipidus 
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease 1  
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease 2  
nephrogenic diabetes insipidus +   
neurohypophyseal diabetes insipidus +   
A genetic or acquired polyuric disorder caused by a deficiency of VASOPRESSINS secreted by the NEUROHYPOPHYSIS. Clinical signs include the excretion of large volumes of dilute URINE; HYPERNATREMIA; THIRST; and polydipsia. Etiologies include HEAD TRAUMA; surgeries and diseases involving the HYPOTHALAMUS and the PITUITARY GLAND. This disorder may also be caused by mutations of genes such as ARVP encoding vasopressin and its corresponding neurophysin (NEUROPHYSINS).
opisthorchiasis  
pancreatic agenesis +   
Pancreatic Cyst +   
Pancreatic Fistula  
pancreatic hypoplasia-diabetes-congenital heart disease syndrome  
Pancreatic Lipase Deficiency  
Pancreatic Lipomatosis Duodenal Stenosis 
pancreatic mucinous ductal ectasia 
Pancreatic Neoplasms +   
pancreatic steatorrhea 
pancreatitis +   
renal-hepatic-pancreatic dysplasia +   
Schofer Beetz Bohl Syndrome 
Wolfram syndrome +   

Synonyms
Exact Synonyms: CDI ;   Diabetes Insipidus Cranial Type ;   Diabetes Insipidus Primary Central ;   Diabetes Insipidus Secondary To Vasopressin Deficiency ;   Diabetes Insipidus, Neurohypophyseal Type ;   Neurogenic Diabetes Insipidus ;   Pituitary Diabetes Insipidus ;   Vasopressin Defective Diabetes Insipidus ;   central diabetes insipidus ;   vasopressin deficiency
Narrow Synonyms: DIABETES INSIPIDUS, NEUROHYPOPHYSEAL, AUTOSOMAL RECESSIVE
Primary IDs: MESH:D020790
Alternate IDs: OMIM:125700 ;   OMIM:304900 ;   RDO:0001328
Xrefs: NCI:C84933
Definition Sources: MESH:D020790

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