DiseaseID 18121

常染色体隐性遗传痉挛性共济失调5型

disease

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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: 2Links: 5
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Record Fields

Scalar fields from the final disease record.

Disease Id
18121
Core Entity Id
76468
Source Entity Count
1
Preferred Name
Spastic Ataxia 5, Autosomal Recessive
Name Cn
常染色体隐性遗传痉挛性共济失调5型
Name Pinyin
Chang Ran Se Ti Yin Xing Yi Chuan Jing Luan Xing Gong Ji Shi Tiao 5 Xing
Name En
Spastic Ataxia 5, Autosomal Recessive
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
disease of anatomical entity
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
disease of anatomical entity
Disease Definition
Version
v1,v2
Suppressed
No

Names

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

Name
Spastic Ataxia 5, Autosomal Recessive
Role
preferred
Name
SPAX5
Role
alias
Name
Spastic Ataxia 5
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021367
Omim
614487
Umls
C3280977
Sym Map
SMDE02328
Do Class
DOID:7
Dis Ge Net
C3280977
Umls Sty
T047
Tcmbank Disease
22185

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome