Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 9Target: 12Links: 21
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 9898
- Core Entity Id
- 67033
- Source Entity Count
- 1
- Preferred Name
- Xeroderma Pigmentosum, Variant Form
- Name Cn
- 着色性干皮病变异型
- Name Pinyin
- Zhuo Se Xing Gan Pi Bing Bian Yi Xing
- Name En
- Xeroderma Pigmentosum, Variant Form
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome; Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Xeroderma Pigmentosum, Variant Form
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS009444
Sym Map
SMDE14409
Dis Ge Net
C0432328
Umls Sty
T019T047
Me Sh Class
C04C16C17C18
Tcmbank Disease
20352
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome; Congenital Abnormality
Me Sh Disease Class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Umls Semantic Type Name
Disease or Syndrome; Congenital Abnormality