DiseaseID 1242

常染色体隐性肌源性先天性多关节挛缩症

disease

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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: 1Target: 1Links: 1
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Record Fields

Scalar fields from the final disease record.

Disease Id
1242
Core Entity Id
1402
Source Entity Count
1
Preferred Name
Autosomal Recessive Myogenic Arthrogryposis Multiplex Congenita
Name Cn
常染色体隐性肌源性先天性多关节挛缩症
Name Pinyin
Chang Ran Se Ti Yin Xing Ji Yuan Xing Xian Tian Xing Duo Guan Jie Luan Suo Zheng
Name En
Autosomal recessive myogenic arthrogryposis multiplex congenita
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
Autosomal Recessive Myogenic Arthrogryposis Multiplex Congenita
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS027713
Dis Ge Net
C4707155
Umls Sty
T047
Tcmbank Disease
22180

Attributes

Merged source attributes and domain-specific metadata.

Disease Type
disease
Umls Disease Type
Disease or Syndrome
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome