| Descriptor English: | Diabetes Insipidus, Neurogenic | ||||||
| Descriptor Spanish: |
Diabetes Insípida Neurogénica
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| Descriptor Portuguese: | Diabetes Insípido Neurogênico | ||||||
| Descriptor French: | Diabète insipide central | ||||||
| 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 |
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| 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 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D020790 | ||||||
| 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). |
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| Annotation: | do not confuse with DIABETES INSIPIDUS, NEPHROGENIC |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Diabetes Insipidus (1966-1999) |
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| Public MeSH Note: | 2000 |
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| History Note: | 2000 |
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| DeCS ID: | 34283 | ||||||
| Unique ID: | D020790 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2000/01/01 | ||||||
| Date of Entry: | 1999/11/03 | ||||||
| Revision Date: | 2013/07/08 |
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Diabetes Insipidus, Neurogenic
- Preferred
| Concept UI |
M0328375 |
| 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). |
| Preferred term | Diabetes Insipidus, Neurogenic |
| 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 |
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