DiseaseID 26412

常染色体显性遗传痉挛性共济失调1型

Spastic Ataxia 1, Autosomal Dominant

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Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Symptom: 3Target: 3Links: 6
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Record Fields

Scalar fields from the final disease record.

Disease Id
26412
Core Entity Id
118980
Source Entity Count
1
Preferred Name
Spastic Ataxia 1, Autosomal Dominant
Name Cn
常染色体显性遗传痉挛性共济失调1型
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Jing Luan Xing Gong Ji Shi Tiao 1 Xing
Name En
Spastic Ataxia 1, Autosomal Dominant
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
v1,v2
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Spastic Ataxia 1, Autosomal Dominant
Role
preferred
Source
SymMap_v2
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Umls
C1970107
Sym Map
SMDE03338

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0