DiseaseID 25867
常染色体遗传性肾性尿崩症
Diabetes Insipidus, Nephrogenic, Autosomal
MSH2017_2016_08_12:Congenital nephrogenic diabetes insipidus associated with mutations of AQUAPORIN-2.
Relationship Network
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Disease: 1Symptom: 10Target: 16Links: 34
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25867
- Core Entity Id
- 118435
- Source Entity Count
- 1
- Preferred Name
- Diabetes Insipidus, Nephrogenic, Autosomal
- Name Cn
- 常染色体遗传性肾性尿崩症
- Name Pinyin
- Chang Ran Se Ti Yi Chuan Xing Shen Xing Niao Beng Zheng
- Name En
- Diabetes Insipidus, Nephrogenic, Autosomal
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- MSH2017_2016_08_12:Congenital nephrogenic diabetes insipidus associated with mutations of AQUAPORIN-2.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Diabetes Insipidus, Nephrogenic, Autosomal
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C1563706
Sym Map
SMDE00730
Etcm Disease
Diabetes Insipidus, Nephrogenic, Autosomal
Itcmdb Generated
ITX-DISEASE-9BAAB069AAE4ITX-DISEASE-C8EFE8599079
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Diabetes Insipidus, Nephrogenic, Autosomal Details page
Basic Information
Disease Name
Diabetes Insipidus, Nephrogenic, Autosomal
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Endocrine diseases;Nephrological diseases;Neuronal diseases
Disease Definition
MSH2017_2016_08_12:Congenital nephrogenic diabetes insipidus associated with mutations of AQUAPORIN-2.