Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Target: 10Links: 10
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 8647
- Core Entity Id
- 65611
- Source Entity Count
- 1
- Preferred Name
- Autosomal Dominant Retinitis Pigmentosa
- Name Cn
- 常染色体显性视网膜色素变性
- Name Pinyin
- Chang Ran Se Ti Xian Xing Shi Wang Mo Se Su Bian Xing
- Name En
- Autosomal Dominant Retinitis Pigmentosa
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye 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 Retinitis Pigmentosa
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS007746
Dis Ge Net
C0339525
Umls Sty
T019
Me Sh Class
C11C16
Tcmbank Disease
3652
Attributes
Merged source attributes and domain-specific metadata.
Disease Type
disease
Umls Disease Type
Congenital Abnormality
Me Sh Disease Class
Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Umls Semantic Type Name
Congenital Abnormality