DiseaseID 2623

常染色体隐性脊髓小脑性共济失调15型 (SCAR15)

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: 4Target: 1Links: 5
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Record Fields

Scalar fields from the final disease record.

Disease Id
2623
Core Entity Id
2973
Source Entity Count
1
Preferred Name
Spinocerebellar Ataxia, Autosomal Recessive 15
Name Cn
常染色体隐性脊髓小脑性共济失调15型 (SCAR15)
Name Pinyin
Chang Ran Se Ti Yin Xing Ji Sui Xiao Nao Xing Gong Ji Shi Tiao 15 Xing (scar15)
Name En
Autosomal Recessive Spinocerebellar Ataxia 15 (SCAR15)
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 15
Role
preferred
Name
Autosomal Recessive Spinocerebellar Ataxia 15
Role
alias
Name
SALIH ATAXIA
Role
alias
Name
SCAR15
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS029515
Omim
615705
Umls
C3810326
Sym Map
SMDE04732
Do Class
DOID:630DOID:7
Dis Ge Net
C3810326
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