DiseaseID 4270
V型高脂蛋白血症
disease
MSH2017_2016_08_12:A severe type of hyperlipidemia, sometimes familial, that is characterized by the elevation of both plasma CHYLOMICRONS and TRIGLYCERIDES contained in VERY-LOW-DENSITY LIPOPROTEINS. Type V hyperlipopro
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Disease: 1Formula: 12Herb: 12Target: 19Links: 48
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4270
- Core Entity Id
- 60593
- Source Entity Count
- 1
- Preferred Name
- Hyperlipoproteinemia Type V
- Name Cn
- V型高脂蛋白血症
- Name Pinyin
- V Xing Gao Zhi Dan Bai Xue Zheng
- Name En
- Hyperlipoproteinemia Type V
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Do Class
- genetic disease; disease of metabolism
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Hpo Class Name
- Do Class Name
- disease of metabolism; genetic disease
- Disease Definition
- MSH2017_2016_08_12:A severe type of hyperlipidemia, sometimes familial, that is characterized by the elevation of both plasma CHYLOMICRONS and TRIGLYCERIDES contained in VERY-LOW-DENSITY LIPOPROTEINS. Type V hyperlipoproteinemia is often associated with DIABETES MELLITUS and is not caused by reduced LIPOPROTEIN LIPASE activity as in HYPERLIPOPROTEINEMIA TYPE I .
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hyperlipoproteinemia Type V
Role
preferred
Name
Hyperlipoproteinemia, Type V
Role
preferred
Name
Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial
Role
preferred
Name
Familial Apolipoprotein A5 Deficiency
Role
alias
Name
HYPERCHYLOMICRONEMIA, LATE-ONSET
Role
alias
Name
HYPERLIPEMIA, COMBINED FAT AND CARBOHYDRATE-INDUCED
Role
alias
Name
HYPERLIPEMIA, MIXED
Role
alias
Name
HYPERLIPIDEMIA, TYPE V
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS001441HBDIS021432
Me Sh
D006954
Omim
144650
Umls
C0020481C3489395
Sym Map
SMDE02625
Do Class
DOID:0014667DOID:630
Dis Ge Net
C0020481C3489395
Umls Sty
T047
Me Sh Class
C16C18
Etcm Disease
Hyperlipoproteinemia, Type V
Tcmbank Disease
172822748
Itcmdb Generated
ITX-DISEASE-2EEE93C08A92ITX-DISEASE-9923E2497AD1
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Hyperlipoproteinemia, Type V Details page
Do Class Name
disease of metabolism; genetic disease
Disease Type
disease
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Hyperlipoproteinemia, Type V
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Blood diseases;Endocrine diseases;Liver diseases;Respiratory diseases
Disease Definition
MSH2017_2016_08_12:A severe type of hyperlipidemia, sometimes familial, that is characterized by the elevation of both plasma CHYLOMICRONS and TRIGLYCERIDES contained in VERY-LOW-DENSITY LIPOPROTEINS. Type V hyperlipoproteinemia is often associated with DIABETES MELLITUS and is not caused by reduced LIPOPROTEIN LIPASE activity as in HYPERLIPOPROTEINEMIA TYPE I .
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome