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
- 13970
- Core Entity Id
- 71690
- Source Entity Count
- 1
- Preferred Name
- Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant
- Name Cn
- 儿童近端脊髓性肌萎缩症,常染色体显性遗传
- Name Pinyin
- Er Tong Jin Duan Ji Sui Xing Ji Wei Suo Zheng , Chang Ran Se Ti Xian Xing Yi Chuan
- Name En
- Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant
- 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
Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant
Role
preferred
Name
Spinal Muscular Atrophy, Lower Extremity-Predominant, 1, Autosomal Dominant
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS015261
Omim
158600
Dis Ge Net
C1834690
Umls Sty
T047
Me Sh Class
C10C16
Tcmbank Disease
26733
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