Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Target: 18Links: 24
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 22124
- Core Entity Id
- 80915
- Source Entity Count
- 1
- Preferred Name
- Dystonia, Childhood-Onset, With Optic Atrophy And Basal Ganglia Abnormalities
- Name Cn
- 儿童期起病的肌张力障碍伴视神经萎缩和基底节异常
- Name Pinyin
- Er Tong Qi Qi Bing De Ji Zhang Li Zhang Ai Ban Shi Shen Jing Wei Suo He Ji Di Jie Yi Chang
- Name En
- Dystonia, Childhood-Onset, With Optic Atrophy And Basal Ganglia Abnormalities
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- 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, Childhood-Onset, With Optic Atrophy And Basal Ganglia Abnormalities
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS026229
Omim
617282
Dis Ge Net
C4310634
Umls Sty
T047
Etcm Disease
Dystonia, Childhood-Onset, with Optic Atrophy and Basal Ganglia Abnormalities
Tcmbank Disease
17278
Itcmdb Generated
ITX-DISEASE-A30D4FE20AB4
Attributes
Merged source attributes and domain-specific metadata.
Page Title
Disease Dystonia, Childhood-Onset, with Optic Atrophy and Basal Ganglia Abnormalities Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Dystonia, Childhood-Onset, with Optic Atrophy and Basal Ganglia Abnormalities
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Eye diseases;Neuronal diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome