DiseaseID 26081
常染色体隐性遗传多囊肾病
Polycystic Kidney Disease, Autosomal Recessive
NCI2016_02D:A congenital disorder usually inherited in an autosomal recessive pattern. It affects the hepatobiliary system and the kidneys. It is characterized by liver fibrosis, portal hypertension, and renal cysts.|HPO
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Disease: 1Symptom: 1Target: 12Links: 13
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26081
- Core Entity Id
- 118649
- Source Entity Count
- 1
- Preferred Name
- Polycystic Kidney Disease, Autosomal Recessive
- Name Cn
- 常染色体隐性遗传多囊肾病
- Name Pinyin
- Chang Ran Se Ti Yin Xing Yi Chuan Duo Nang Shen Bing
- Name En
- Polycystic Kidney Disease, Autosomal Recessive
- 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
- NCI2016_02D:A congenital disorder usually inherited in an autosomal recessive pattern. It affects the hepatobiliary system and the kidneys. It is characterized by liver fibrosis, portal hypertension, and renal cysts.|HPO2016_07_04:The presence of fibrosis of that part of the liver with congenital onset. [HPO:probinson]
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Polycystic Kidney Disease, Autosomal Recessive
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Umls
C0009714
Sym Map
SMDE01864
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Definition
NCI2016_02D:A congenital disorder usually inherited in an autosomal recessive pattern. It affects the hepatobiliary system and the kidneys. It is characterized by liver fibrosis, portal hypertension, and renal cysts.|HPO2016_07_04:The presence of fibrosis of that part of the liver with congenital onset. [HPO:probinson]