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Diabetes Insipidus, Neurogenic MeSH Descriptor Data 2024


MeSH Heading
Diabetes Insipidus, Neurogenic
Tree Number(s)
C12.050.351.968.419.135.750
C12.200.777.419.135.750
C12.950.419.135.750
C19.700.159.750
Unique ID
D020790
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D020790
Annotation
do not confuse with DIABETES INSIPIDUS, NEPHROGENIC
Scope Note
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).
Entry Term(s)
Central Diabetes Insipidus
Diabetes Insipidus Cranial Type
Diabetes Insipidus Primary Central
Diabetes Insipidus Secondary To Vasopressin Deficiency
Diabetes Insipidus, Central
Diabetes Insipidus, Cranial Type
Diabetes Insipidus, Neurohypophyseal
Diabetes Insipidus, Neurohypophyseal Type
Diabetes Insipidus, Pituitary
Diabetes Insipidus, Primary Central
Neurogenic Diabetes Insipidus
Neurohypophyseal Diabetes Insipidus
Pituitary Diabetes Insipidus
Vasopressin Defective Diabetes Insipidus
Vasopressin Deficiency
Previous Indexing
Diabetes Insipidus (1966-1999)
Public MeSH Note
2000
History Note
2000
Date Established
2000/01/01
Date of Entry
1999/11/03
Revision Date
2021/06/30
Diabetes Insipidus, Neurogenic Preferred
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