DiseaseID 21626

常染色体显性遗传小脑性共济失调

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: 1Target: 18Links: 24
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Record Fields

Scalar fields from the final disease record.

Disease Id
21626
Core Entity Id
80362
Source Entity Count
1
Preferred Name
Autosomal Dominant Cerebellar Ataxia
Name Cn
常染色体显性遗传小脑性共济失调
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Xiao Nao Xing Gong Ji Shi Tiao
Name En
Autosomal Dominant Cerebellar Ataxia
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
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
Autosomal Dominant Cerebellar Ataxia
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS025591
Dis Ge Net
C4087347
Umls Sty
T047
Etcm Disease
Autosomal Dominant Cerebellar Ataxia
Tcmbank Disease
19584
Itcmdb Generated
ITX-DISEASE-1B06A71B36FE

Attributes

Merged source attributes and domain-specific metadata.

Page Title
Disease Autosomal Dominant Cerebellar Ataxia Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Autosomal Dominant Cerebellar Ataxia
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Neuronal diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome