DiseaseID 13637
硫脂沉积症
disease
MSH2017_2016_08_12:A group of inherited metabolic disorders characterized by the intralysosomal accumulation of sulfur-containing lipids (SULFATIDES), including SULFOGLYCOSPHINGOLIPIDS normally found in the MYELIN SHEATH
Relationship Network
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Disease: 1Symptom: 6Target: 11Links: 17
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 13637
- Core Entity Id
- 71310
- Source Entity Count
- 1
- Preferred Name
- Sulfatidosis
- Name Cn
- 硫脂沉积症
- Name Pinyin
- Liu Zhi Chen Ji Zheng
- Name En
- Sulfatidosis
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- MSH2017_2016_08_12:A group of inherited metabolic disorders characterized by the intralysosomal accumulation of sulfur-containing lipids (SULFATIDES), including SULFOGLYCOSPHINGOLIPIDS normally found in the MYELIN SHEATH of the brain. These disorders are caused by defective degradative enzymes leading to substrate accumulation (or storage).
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Sulfatidosis
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS014775
Me Sh
D052516
Umls
C1706192
Sym Map
SMDE13728
Dis Ge Net
C1706192
Umls Sty
T047
Me Sh Class
C10C16C18
Tcmbank Disease
29679
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disease Definition
MSH2017_2016_08_12:A group of inherited metabolic disorders characterized by the intralysosomal accumulation of sulfur-containing lipids (SULFATIDES), including SULFOGLYCOSPHINGOLIPIDS normally found in the MYELIN SHEATH of the brain. These disorders are caused by defective degradative enzymes leading to substrate accumulation (or storage).
Me Sh Disease Class
Nervous System Diseases; 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; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome