DiseaseID 4486
类脂沉积症
disease
MSH2017_2016_08_12:Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified e
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Disease: 1Symptom: 9Target: 12Links: 21
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4486
- Core Entity Id
- 60841
- Source Entity Count
- 2
- Preferred Name
- Lipoidosis
- Name Cn
- 类脂沉积症
- Name Pinyin
- Lei Zhi Chen Ji Zheng
- Name En
- Lipoidosis
- 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 DiseasesNutritional 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 DiseasesNutritional and Metabolic Diseases
- Hpo Class Name
- Do Class Name
- disease of metabolism; genetic disease
- Disease Definition
- MSH2017_2016_08_12:Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved.|CSP2006:disturbance of lipid metabolism with abnormal deposit of lipids in the cells.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Lipoidosis
Role
preferred
Name
Other Disorders of Lipoid Metabolism
Role
preferred
Name
Lipid Storage Disease
Role
alias
Name
Lipid Storage Disorder, Unspecified
Role
alias
Name
Lipidoses
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS001752HBDIS002238
Me Sh
D008064
Umls
C0023794
Icd10
E75.6
Sym Map
SMDE10463
Do Class
DOID:0014667DOID:630
Dis Ge Net
C0023794C0029591
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
2417961526990
Itcmdb Generated
ITX-DISEASE-41B71E5FDED6
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
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
Disease Definition
MSH2017_2016_08_12:Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved.|CSP2006:disturbance of lipid metabolism with abnormal deposit of lipids in the cells.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic DiseasesNutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic DiseasesNutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome