DiseaseID 32001
伴糖基化缺陷的先天性肌无力综合征
Congenital Myasthenic Syndromes with Glycosylation Defect
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 1Herb: 5Target: 21Links: 30
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 32001
- Core Entity Id
- 191935
- Source Entity Count
- 1
- Preferred Name
- Congenital Myasthenic Syndromes with Glycosylation Defect
- Name Cn
- 伴糖基化缺陷的先天性肌无力综合征
- Name Pinyin
- Ban Tang Ji Hua Que Xian De Xian Tian Xing Ji Wu Li Zong He Zheng
- Name En
- Congenital Myasthenic Syndromes with Glycosylation Defect
- 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
- Version
- Suppressed
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Congenital Myasthenic Syndromes with Glycosylation Defect
Role
preferred
Source
ETCM_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Etcm Disease
Congenital Myasthenic Syndromes with Glycosylation Defect
Itcmdb Generated
ITX-DISEASE-033B3E8929DC
Attributes
Merged source attributes and domain-specific metadata.
Page Title
Disease Congenital Myasthenic Syndromes with Glycosylation Defect Details page
Basic Information
Disease Name
Congenital Myasthenic Syndromes with Glycosylation Defect
Global Category
Fetal diseases;Metabolic diseases;Rare diseases
Anatomical Category
Eye diseases;Neuronal diseases