DiseaseID 2907

常染色体隐性遗传脊髓小脑共济失调21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: 1Target: 2Links: 3
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Record Fields

Scalar fields from the final disease record.

Disease Id
2907
Core Entity Id
3291
Source Entity Count
1
Preferred Name
Spinocerebellar Ataxia, Autosomal Recessive 21
Name Cn
常染色体隐性遗传脊髓小脑共济失调21型
Name Pinyin
Chang Ran Se Ti Yin Xing Yi Chuan Ji Sui Xiao Nao Gong Ji Shi Tiao 21 Xing
Name En
Spinocerebellar Ataxia, Autosomal Recessive 21
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
Suppressed
No

Names

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

Name
Spinocerebellar Ataxia, Autosomal Recessive 21
Role
preferred
Name
Autosomal Recessive Spinocerebellar Ataxia 21
Role
alias
Name
SCAR21
Role
alias
Name
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21, WITH HEPATOPATHY
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS029842
Omim
616719
Umls
C4225236
Sym Map
SMDE00262
Do Class
DOID:630DOID:7
Dis Ge Net
C4225236
Umls Sty
T047

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
Dis Ge Net Disease Type
disease