DiseaseID 2481

10型常染色体隐性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: 5Links: 7
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
2481
Core Entity Id
2804
Source Entity Count
1
Preferred Name
Spinocerebellar Ataxia, Autosomal Recessive 10
Name Cn
10型常染色体隐性脊髓小脑性共济失调
Name Pinyin
10 Xing Chang Ran Se Ti Yin Xing Ji Sui Xiao Nao Xing Gong Ji Shi Tiao
Name En
Autosomal Recessive Spinocerebellar Ataxia 10
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
disease of anatomical entity; genetic disease
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
v1,v2
Suppressed
No

Names

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

Name
Spinocerebellar Ataxia, Autosomal Recessive 10
Role
preferred
Name
Autosomal Recessive Spinocerebellar Ataxia 10
Role
alias
Name
SCAR10
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS029269
Omim
613728
Umls
C3150998
Sym Map
SMDE04102
Do Class
DOID:630DOID:7
Dis Ge Net
C3150998
Umls Sty
T047

Attributes

Merged source attributes and domain-specific metadata.

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