DiseaseID 2668

脊髓小脑性共济失调常染色体隐性17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: 2Target: 1Links: 3
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
2668
Core Entity Id
3026
Source Entity Count
1
Preferred Name
Spinocerebellar Ataxia, Autosomal Recessive 17
Name Cn
脊髓小脑性共济失调常染色体隐性17型
Name Pinyin
Ji Sui Xiao Nao Xing Gong Ji Shi Tiao Chang Ran Se Ti Yin Xing 17 Xing
Name En
Spinocerebellar Ataxia, Autosomal Recessive 17
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 17
Role
preferred
Name
Autosomal Recessive Spinocerebellar Ataxia 17
Role
alias
Name
SCAR17
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS029585
Omim
616127
Umls
C4015301
Sym Map
SMDE00023
Do Class
DOID:630DOID:7
Dis Ge Net
C4015301
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