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
- 22059
- Core Entity Id
- 80840
- Source Entity Count
- 1
- Preferred Name
- Autosomal Dominant Beta2-Microglobulinic Amyloidosis
- Name Cn
- 常染色体显性遗传性β2-微球蛋白淀粉样变性
- Name Pinyin
- Chang Ran Se Ti Xian Xing Yi Chuan Xing Β2- Wei Qiu Dan Bai Dian Fen Yang Bian Xing
- Name En
- Autosomal Dominant Beta2-Microglobulinic Amyloidosis
- 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; Nutritional and Metabolic Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic 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 Beta2-Microglobulinic Amyloidosis
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS026139
Dis Ge Net
C4302669
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
31276
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; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome