DiseaseID 1243

KIF5A突变引起的常染色体显性遗传腓骨肌萎缩症2型

disease

Back to Browse

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: 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