DiseaseID 1508

常染色体显性遗传儿童期发病2A型以下肢为主的脊髓性肌萎缩症

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
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
1508
Core Entity Id
1699
Source Entity Count
1
Preferred Name
Spinal Muscular Atrophy, Lower Extremity-Predominant, 2A, Childhood Onset, Autosomal Dominant
Name Cn
常染色体显性遗传儿童期发病2A型以下肢为主的脊髓性肌萎缩症
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Er Tong Qi Fa Bing 2a Xing Yi Xia Zhi Wei Zhu De Ji Sui Xing Ji Wei Suo Zheng
Name En
Spinal Muscular Atrophy, Lower Extremity-Predominant, 2A, Childhood 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, 2A, Childhood Onset, Autosomal Dominant
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS028015
Omim
615290
Dis Ge Net
C4747715
Umls Sty
T047
Tcmbank Disease
25810

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