DiseaseID 2637

脊髓小脑性共济失调35型 (SCA35)

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: 1Target: 2Links: 3
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Record Fields

Scalar fields from the final disease record.

Disease Id
2637
Core Entity Id
2989
Source Entity Count
1
Preferred Name
Spinocerebellar Ataxia 35
Name Cn
脊髓小脑性共济失调35型 (SCA35)
Name Pinyin
Ji Sui Xiao Nao Xing Gong Ji Shi Tiao 35 Xing (sca35)
Name En
Spinocerebellar Ataxia 35 (SCA35)
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
v1
Suppressed
No

Names

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

Name
Spinocerebellar Ataxia 35
Role
preferred
Name
SCA35
Role
alias
Name
Spinocerebellar Ataxia Type 35
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS029533
Omim
613908
Umls
C3888031
Sym Map
SMDE03673
Do Class
DOID:630DOID:7
Dis Ge Net
C3888031
Umls Sty
T047
Me Sh Class
C10C16

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
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