DiseaseID 26301

常染色体显性遗传痉挛性截瘫17型

Spastic Paraplegia 17, Autosomal Dominant

Back to Browse

Relationship Network

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

Click a node to open it in a new tab
Disease: 1Target: 4Links: 4
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
26301
Core Entity Id
118869
Source Entity Count
1
Preferred Name
Spastic Paraplegia 17, Autosomal Dominant
Name Cn
常染色体显性遗传痉挛性截瘫17型
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Jing Luan Xing Jie Tan 17 Xing
Name En
Spastic Paraplegia 17, 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
Suppressed
No

Names

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

Name
Spastic Paraplegia 17, Autosomal Dominant
Role
preferred
Source
SymMap_v2
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Umls
C2931276
Sym Map
SMDE02879

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0