Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Herb: 2Target: 17Links: 26
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3026
- Core Entity Id
- 3424
- Source Entity Count
- 1
- Preferred Name
- Arthrogryposis Multiplex Congenita, Neurogenic, With Myelin Defect
- Name Cn
- 神经源性先天性多关节挛缩伴髓鞘缺陷
- Name Pinyin
- Shen Jing Yuan Xing Xian Tian Xing Duo Guan Jie Luan Suo Ban Sui Qiao Que Xian
- Name En
- Neurogenic Arthrogryposis Multiplex Congenita with Myelin Defect
- Name Latin
- Bilingual Status
- complete
- Disease Type
- 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
Arthrogryposis Multiplex Congenita, Neurogenic, With Myelin Defect
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS029988
Omim
617468
Dis Ge Net
C4479539
Umls Sty
T047
Etcm Disease
Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect
Itcmdb Generated
ITX-DISEASE-1474D28BA47F
Attributes
Merged source attributes and domain-specific metadata.
Page Title
Disease Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Details page
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect
Global Category
Fetal diseases;Genetic diseases
Anatomical Category
Muscle diseases;Neuronal diseases
Dis Ge Net Disease Type
disease