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

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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