DiseaseID 32283

常染色体显性遗传扭转性肌张力障碍13型

Dystonia 13, Torsion, Autosomal Dominant

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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: 1Formula: 8Herb: 12Target: 17Links: 44
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
32283
Core Entity Id
192217
Source Entity Count
1
Preferred Name
Dystonia 13, Torsion, Autosomal Dominant
Name Cn
常染色体显性遗传扭转性肌张力障碍13型
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Niu Zhuan Xing Ji Zhang Li Zhang Ai 13 Xing
Name En
Dystonia 13, Torsion, Autosomal Dominant
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disgenet Type
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
Suppressed

Names

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

Name
Dystonia 13, Torsion, Autosomal Dominant
Role
preferred
Source
ETCM_v2
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Etcm Disease
Dystonia 13, Torsion, Autosomal Dominant
Itcmdb Generated
ITX-DISEASE-B3D468693A70

Attributes

Merged source attributes and domain-specific metadata.

Page Title
Disease Dystonia 13, Torsion, Autosomal Dominant Details page
Basic Information
Disease Name
Dystonia 13, Torsion, Autosomal Dominant
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Muscle diseases;Neuronal diseases