DiseaseID 18096

常染色体隐性脊髓小脑共济失调12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: 5Target: 2Links: 7
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Record Fields

Scalar fields from the final disease record.

Disease Id
18096
Core Entity Id
76435
Source Entity Count
1
Preferred Name
Spinocerebellar Ataxia, Autosomal Recessive 12
Name Cn
常染色体隐性脊髓小脑共济失调12型
Name Pinyin
Chang Ran Se Ti Yin Xing Ji Sui Xiao Nao Gong Ji Shi Tiao 12 Xing
Name En
Spinocerebellar Ataxia, Autosomal Recessive 12
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 12
Role
preferred
Name
Autosomal Recessive Spinocerebellar Ataxia 12
Role
alias
Name
SCAR12
Role
alias
Name
SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021300
Omim
614322
Umls
C3280452
Sym Map
SMDE00128
Do Class
DOID:630DOID:7
Dis Ge Net
C3280452
Umls Sty
T047
Tcmbank Disease
31055

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