DiseaseID 3796

尿崩症

disease

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Disease: 1Formula: 5Symptom: 8Target: 21Links: 37

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Record Fields

Scalar fields from the final disease record.

Disease Id: 3796
Core Entity Id: 60046
Source Entity Count: 1
Preferred Name: Diabetes Insipidus
Name Cn: 尿崩症
Name Pinyin: Niao Beng Zheng
Name En: Diabetes Insipidus
Name Latin
Bilingual Status: complete
Disease Type: disease
Umls Disease Type: Disease or Syndrome
Disgenet Type: disease
Mesh Class: Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
Do Class: disease of anatomical entity
Hpo Class: Abnormality of the endocrine systemAbnormality of the nervous system; Abnormality of the endocrine system
Mesh Class Name: Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
Hpo Class Name: Abnormality of the endocrine system
Do Class Name: disease of anatomical entity
Disease Definition: Hereditary central diabetes insipidus is a rare genetic subtype of central diabetes insipidus (CDI, see this term) characterized by polyuria and polydipsia due to a deficiency in vasopressin (AVP) syn
Version: v1
Suppressed: No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name

Diabetes Insipidus

Role

preferred

Name

Central Diabetes Insipidus

Role

preferred

Name

Hereditary Central Diabetes Insipidus

Role

preferred

Name

Diabetes Insipidus, Neurogenic

Role

alias

Name

Diabetes Insipidus, Neurohypophyseal

Role

alias

Name

Diabetes Insipidus, Neurohypophyseal Type

Role

alias

Name

Neurohypophyseal Diabetes Insipidus

Role

alias

Cross References

Trusted external identifiers retained for this final record.

Hpo

HP:0000863HP:0000873

Herb

HBDIS000773HBDIS010639

Me Sh

D003919D020790

Omim

125700304900

Umls

C0011848

Icd10

E23.2

Sym Map

SMDE00716SMDE07849

Do Class

DOID:7

Dis Ge Net

C0011848C0687720

Orphanet

30925

Umls Sty

T047

Hpo Class

HP:0000707HP:0000818

Me Sh Class

C12C13C19

Etcm Disease

Hereditary Central Diabetes Insipidus

Tcmbank Disease

184256236896

Itcmdb Generated

ITX-DISEASE-00CFEDA86301ITX-DISEASE-5DC5C5E384DDITX-DISEASE-9133940A173B

Attributes

Merged source attributes and domain-specific metadata.

Version

v1v2

Suppress

Page Title

Disease Hereditary Central Diabetes Insipidus Details page

Do Class Name

disease of anatomical entity

Disease Type

disease

Hpo Class Name

Abnormality of the endocrine system

Do Disease Class

disease of anatomical entity

Hpo Disease Class

Abnormality of the endocrine systemAbnormality of the nervous system; Abnormality of the endocrine system

Umls Disease Type

Disease or Syndrome

Basic Information

Disease Name

Hereditary Central Diabetes Insipidus

Global Category

Rare diseases

Anatomical Category

Endocrine diseases;Nephrological diseases;Neuronal diseases

Disease Definition

Hereditary central diabetes insipidus is a rare genetic subtype of central diabetes insipidus (CDI, see this term) characterized by polyuria and polydipsia due to a deficiency in vasopressin (AVP) synNCI2016_NICHD_1602D:A disorder characterized by excretion of large amounts of dilute urine, accompanied by excessive thirst. Causes include deficiency of antidiuretic hormone or failure of the kidneys to respond to antidiuretic hormone.|NCI2016_02D:A disorder characterized by excretion of large amounts of urine, accompanied by excessive thirst. Causes include deficiency of antidiuretic hormone or failure of the kidneys to respond to antidiuretic hormone. It may also be drug-related.|MSH2017_2016_08_12:A disease that is characterized by frequent urination, excretion of large amounts of dilute URINE, and excessive THIRST. Etiologies of diabetes insipidus include deficiency of antidiuretic hormone (also known as ADH or VASOPRESSIN) secreted by the NEUROHYPOPHYSIS, impaired KIDNEY response to ADH, and impaired hypothalamic regulation of thirst.|MEDLINEPLUS_20151021:Diabetes insipidus (DI) causes frequent urination. You become extremely thirsty, so you drink. Then you urinate. This cycle can keep you from sleeping or even make you wet the bed. Your body produces lots of urine that is almost all water. DI is different from <a href='https://www.nlm.nih.gov/medlineplus/diabetes.html'>diabetes</a> mellitus (DM), which involves insulin problems and high blood sugar. The symptoms can be similar. However, DI is related to how your kidneys handle fluids. It's much less common than DM. Urine and blood tests can show which one you have. Usually, DI is caused by a problem with your pituitary gland or your kidneys. Treatment depends on the cause of the problem. Medicines can often help. NIH: National Institute of Diabetes and Digestive and Kidney Diseases|HPO2016_07_04:A state of excessive water intake and hypotonic (dilute) polyuria. Diabetes insipidus may be due to failure of vasopressin (AVP) release (central or neurogenic diabetes insipidus) or to a failure of the kidney to respond to AVP (nephrogenic diabetes insipidus). [HPO:curators]|CSP2006:metabolic disorder due to injury of the neurohypophyseal system; results in deficient quanity of antidiuretic hormone being released or produced, failure of tubular reabsorption of water in the kidney.|CHV2011_02:a lack of antidiuretic hormone that causes excessive production of very dilute urine|CHV2011_02:a lack of antidiuretic hormone that causes excessive production of very dilute urine|CHV2011_02:A disease that is characterized by frequent urination, excretion of large amounts of dilute URINE, and excessive THIRST.

Me Sh Disease Class

Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases

Dis Ge Net Disease Type

disease

Disease Class Name Me Sh

Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases

Umls Semantic Type Name

Disease or Syndrome