DiseaseID 26279

常染色体显性遗传痉挛性截瘫12型

Spastic Paraplegia 12, 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: 1Target: 10Links: 11
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Record Fields

Scalar fields from the final disease record.

Disease Id
26279
Core Entity Id
118847
Source Entity Count
1
Preferred Name
Spastic Paraplegia 12, Autosomal Dominant
Name Cn
常染色体显性遗传痉挛性截瘫12型
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Jing Luan Xing Jie Tan 12 Xing
Name En
Spastic Paraplegia 12, 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 Paraplegia 12, Autosomal Dominant
Role
preferred
Source
SymMap_v2
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Umls
C1858106
Sym Map
SMDE02788

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0