DiseaseID 29033
遗传性中枢神经系统脱髓鞘疾病
Hereditary Central Nervous System Demyelinating Diseases
MSH2017_2016_08_12:Inherited conditions characterized by a loss of MYELIN in the central nervous system.
Relationship Network
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Disease: 1Symptom: 4Target: 12Links: 16
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 29033
- Core Entity Id
- 121601
- Source Entity Count
- 1
- Preferred Name
- Hereditary Central Nervous System Demyelinating Diseases
- Name Cn
- 遗传性中枢神经系统脱髓鞘疾病
- Name Pinyin
- Yi Chuan Xing Zhong Shu Shen Jing Xi Tong Tuo Sui Qiao Ji Bing
- Name En
- Hereditary Central Nervous System Demyelinating Diseases
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- MSH2017_2016_08_12:Inherited conditions characterized by a loss of MYELIN in the central nervous system.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hereditary Central Nervous System Demyelinating Diseases
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Me Sh
D020279
Umls
C0751877
Sym Map
SMDE09411
Itcmdb Generated
ITX-DISEASE-DEAE634DC220
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Definition
MSH2017_2016_08_12:Inherited conditions characterized by a loss of MYELIN in the central nervous system.