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
- 1243
- Core Entity Id
- 1403
- Source Entity Count
- 1
- Preferred Name
- Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Kif5A Mutation
- Name Cn
- KIF5A突变引起的常染色体显性遗传腓骨肌萎缩症2型
- Name Pinyin
- Kif5a Tu Bian Yin Qi De Chang Ran Se Ti Xian Xing Yi Chuan Fei Gu Ji Wei Suo Zheng 2 Xing
- Name En
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
- 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
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- Suppressed
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Kif5A Mutation
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS027714
Dis Ge Net
C4707173
Umls Sty
T047
Me Sh Class
C10C16
Tcmbank Disease
15696
Attributes
Merged source attributes and domain-specific metadata.
Disease Type
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