DiseaseID 14558

脊髓小脑性共济失调18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: 1Links: 1
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
14558
Core Entity Id
72362
Source Entity Count
1
Preferred Name
Spinocerebellar Ataxia 18
Name Cn
脊髓小脑性共济失调18型
Name Pinyin
Ji Sui Xiao Nao Xing Gong Ji Shi Tiao 18 Xing
Name En
Spinocerebellar Ataxia 18
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
Suppressed

Names

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

Name
Spinocerebellar Ataxia 18
Role
preferred
Name
Sensorimotor Neuropathy With Ataxia, Autosomal Dominant
Role
alias
Name
Spinocerebellar Ataxia Type 18
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS016065
Do Class
DOID:630DOID:7
Dis Ge Net
C1843884
Umls Sty
T047
Me Sh Class
C10C16
Tcmbank Disease
21527

Attributes

Merged source attributes and domain-specific metadata.

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