DiseaseID 2211

25型脊髓小脑性共济失调

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: 1Symptom: 2Target: 2Links: 4
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
2211
Core Entity Id
2488
Source Entity Count
1
Preferred Name
Spinocerebellar Ataxia 25
Name Cn
25型脊髓小脑性共济失调
Name Pinyin
25 Xing Ji Sui Xiao Nao Xing Gong Ji Shi Tiao
Name En
Spinocerebellar Ataxia 25
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Do Class
disease of anatomical entity; genetic disease
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
v2
Suppressed
No

Names

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

Name
Spinocerebellar Ataxia 25
Role
preferred
Name
Spinocerebellar Ataxia Type 25
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS028804
Umls
C1837518
Sym Map
SMDE13354
Do Class
DOID:630DOID:7
Dis Ge Net
C1837518
Umls Sty
T047
Me Sh Class
C10C16

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Dis Ge Net Disease Type
disease