DiseaseID 18357

常染色体隐性遗传脊髓小脑性共济失调13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: 4Target: 1Links: 5
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Record Fields

Scalar fields from the final disease record.

Disease Id
18357
Core Entity Id
76744
Source Entity Count
1
Preferred Name
Spinocerebellar Ataxia, Autosomal Recessive 13
Name Cn
常染色体隐性遗传脊髓小脑性共济失调13型
Name Pinyin
Chang Ran Se Ti Yin Xing Yi Chuan Ji Sui Xiao Nao Xing Gong Ji Shi Tiao 13 Xing
Name En
Spinocerebellar Ataxia, Autosomal Recessive 13
Name Latin
Bilingual Status
complete
Disease Type
disease
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
genetic disease; disease of anatomical entity
Disease Definition
Version
v1,v2
Suppressed
No

Names

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

Name
Spinocerebellar Ataxia, Autosomal Recessive 13
Role
preferred
Name
Autosomal Recessive Spinocerebellar Ataxia 13
Role
alias
Name
SCAR13
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021788
Omim
614831
Umls
C3553816
Sym Map
SMDE00652
Do Class
DOID:630DOID:7
Dis Ge Net
C3553816
Umls Sty
T047
Tcmbank Disease
13258

Attributes

Merged source attributes and domain-specific metadata.

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