DiseaseID 18161

脊髓小脑性共济失调36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: 1Target: 11Links: 11
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Record Fields

Scalar fields from the final disease record.

Disease Id
18161
Core Entity Id
76514
Source Entity Count
1
Preferred Name
Spinocerebellar Ataxia 36
Name Cn
脊髓小脑性共济失调36型
Name Pinyin
Ji Sui Xiao Nao Xing Gong Ji Shi Tiao 36 Xing
Name En
Spinocerebellar Ataxia 36
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Do Class
disease of anatomical entity; genetic disease
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Hpo Class Name
Do Class Name
genetic disease; disease of anatomical entity
Disease Definition
Version
v1
Suppressed
No

Names

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

Name
Spinocerebellar Ataxia 36
Role
preferred
Name
SCA36
Role
alias
Name
Spinocerebellar Ataxia Type 36
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021430
Omim
614153
Umls
C3472711
Sym Map
SMDE04126
Do Class
DOID:630DOID:7
Dis Ge Net
C3472711
Umls Sty
T047
Me Sh Class
C10C16
Tcmbank Disease
17028

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
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
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome