DiseaseID 1620

脊髓性肌萎缩症下肢为主型2B型产前发病常染色体显性

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
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
1620
Core Entity Id
1823
Source Entity Count
1
Preferred Name
Spinal Muscular Atrophy, Lower Extremity-Predominant, 2B, Prenatal Onset, Autosomal Dominant
Name Cn
脊髓性肌萎缩症下肢为主型2B型产前发病常染色体显性
Name Pinyin
Ji Sui Xing Ji Wei Suo Zheng Xia Zhi Wei Zhu Xing 2b Xing Chan Qian Fa Bing Chang Ran Se Ti Xian Xing
Name En
Spinal Muscular Atrophy, Lower Extremity-Predominant, 2B, Prenatal Onset, Autosomal Dominant
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
Spinal Muscular Atrophy, Lower Extremity-Predominant, 2B, Prenatal Onset, Autosomal Dominant
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS028129
Omim
618291
Dis Ge Net
C4749003
Umls Sty
T047
Tcmbank Disease
10330

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