DiseaseID 5054
先天性肾小管转运障碍
group
MSH2017_2016_08_12:Genetic defects in the selective or non-selective transport functions of the KIDNEY TUBULES.|CSP2006:genetically determined disorders of the reabsorptive functions of the kidney with regard to specific
Relationship Network
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Disease: 1Symptom: 3Target: 12Links: 15
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5054
- Core Entity Id
- 61494
- Source Entity Count
- 1
- Preferred Name
- Renal Tubular Transport, Inborn Errors
- Name Cn
- 先天性肾小管转运障碍
- Name Pinyin
- Xian Tian Xing Shen Xiao Guan Zhuan Yun Zhang Ai
- Name En
- Renal Tubular Transport, Inborn Errors
- Name Latin
- Bilingual Status
- complete
- Disease Type
- group
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- group
- Mesh Class
- Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:Genetic defects in the selective or non-selective transport functions of the KIDNEY TUBULES.|CSP2006:genetically determined disorders of the reabsorptive functions of the kidney with regard to specific nephron segments responsible for specific transport functions, classifiable by proximal nephron function, loop of Henle function, and distal nephron function; transport defects can be selective or nonselective.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Renal Tubular Transport, Inborn Errors
Role
preferred
Name
Renal Tubular Transport Disease
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS002590
Me Sh
D015499
Umls
C0035091
Sym Map
SMDE12797
Do Class
DOID:7
Dis Ge Net
C0035091
Umls Sty
T047
Me Sh Class
C12C13C16C18
Tcmbank Disease
23699
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
group
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Disease Definition
MSH2017_2016_08_12:Genetic defects in the selective or non-selective transport functions of the KIDNEY TUBULES.|CSP2006:genetically determined disorders of the reabsorptive functions of the kidney with regard to specific nephron segments responsible for specific transport functions, classifiable by proximal nephron function, loop of Henle function, and distal nephron function; transport defects can be selective or nonselective.
Me Sh Disease Class
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
group
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Umls Semantic Type Name
Disease or Syndrome