DiseaseID 5560

肝衰竭

disease

NCI2016_CTCAE_1602D:A disorder characterized by the inability of the liver to metabolize chemicals in the body. Laboratory test results reveal abnormal plasma levels of ammonia, bilirubin, lactic dehydrogenase, and alkal

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Disease: 1Symptom: 11Target: 12Links: 23
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Record Fields

Scalar fields from the final disease record.

Disease Id
5560
Core Entity Id
62080
Source Entity Count
2
Preferred Name
Liver Failure
Name Cn
肝衰竭
Name Pinyin
Gan Shuai Jie
Name En
Liver Failure
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Digestive System Diseases
Do Class
Hpo Class
Abnormality of the digestive system
Mesh Class Name
Digestive System Diseases
Hpo Class Name
Abnormality of the digestive system
Do Class Name
Disease Definition
NCI2016_CTCAE_1602D:A disorder characterized by the inability of the liver to metabolize chemicals in the body. Laboratory test results reveal abnormal plasma levels of ammonia, bilirubin, lactic dehydrogenase, and alkaline phosphatase.|NCI2016_02D:A disorder characterized by the inability of the liver to metabolize chemicals in the body. Causes include cirrhosis and drug-induced hepatotoxicity. Signs and symptoms include jaundice and encephalopathy. Laboratory test results reveal abnormal plasma levels of ammonia, bilirubin, lactic dehydrogenase, and alkaline phosphatase.|MSH2017_2016_08_12:Severe inability of the LIVER to perform its normal metabolic functions, as evidenced by severe JAUNDICE and abnormal serum levels of AMMONIA; BILIRUBIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; LACTATE DEHYDROGENASES; and albumin/globulin ratio. (Blakiston's Gould Medical Dictionary, 4th ed)|CSP2006:severe inability of the liver to function normally, as evidenced by severe jaundice and abnormal levels of ammonia, bilirubin, alkaline phosphatase, glutamic oxaloacetic transaminase, lactic dehydrogenase, and reversal of the albumin/globulin ratio.
Version
v2
Suppressed
No

Names

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

Name
Liver Failure
Role
preferred
Name
Hepatic Failure
Role
alias
Name
Hepatic Failure, Unspecified
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Hpo
HP:0001399
Herb
HBDIS003319
Me Sh
D017093
Umls
C0085605
Icd10
K72.9
Sym Map
SMDE10487
Dis Ge Net
C0085605
Umls Sty
T047
Hpo Class
HP:0025031
Me Sh Class
C06
Tcmbank Disease
103614366
Itcmdb Generated
ITX-DISEASE-E730C028C9BB

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Disease Type
disease
Hpo Class Name
Abnormality of the digestive system
Hpo Disease Class
Abnormality of the digestive system
Umls Disease Type
Disease or Syndrome
Disease Definition
NCI2016_CTCAE_1602D:A disorder characterized by the inability of the liver to metabolize chemicals in the body. Laboratory test results reveal abnormal plasma levels of ammonia, bilirubin, lactic dehydrogenase, and alkaline phosphatase.|NCI2016_02D:A disorder characterized by the inability of the liver to metabolize chemicals in the body. Causes include cirrhosis and drug-induced hepatotoxicity. Signs and symptoms include jaundice and encephalopathy. Laboratory test results reveal abnormal plasma levels of ammonia, bilirubin, lactic dehydrogenase, and alkaline phosphatase.|MSH2017_2016_08_12:Severe inability of the LIVER to perform its normal metabolic functions, as evidenced by severe JAUNDICE and abnormal serum levels of AMMONIA; BILIRUBIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; LACTATE DEHYDROGENASES; and albumin/globulin ratio. (Blakiston's Gould Medical Dictionary, 4th ed)|CSP2006:severe inability of the liver to function normally, as evidenced by severe jaundice and abnormal levels of ammonia, bilirubin, alkaline phosphatase, glutamic oxaloacetic transaminase, lactic dehydrogenase, and reversal of the albumin/globulin ratio.
Me Sh Disease Class
Digestive System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Digestive System Diseases
Umls Semantic Type Name
Disease or Syndrome