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.

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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.