Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 16Herb: 12Symptom: 2Target: 19Links: 54
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 16451
- Core Entity Id
- 74528
- Source Entity Count
- 1
- Preferred Name
- Cavitary Optic Disc Anomalies
- Name Cn
- 空腔性视盘异常
- Name Pinyin
- Kong Qiang Xing Shi Pan Yi Chang
- Name En
- Cavitary Optic Disc Anomalies
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- 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
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Cavitary Optic Disc Anomalies
Role
preferred
Name
CODA
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS018726
Umls
C1969063
Sym Map
SMDE04460
Dis Ge Net
C1969063
Umls Sty
T047
Me Sh Class
C11C16
Etcm Disease
Cavitary Optic Disc Anomalies
Tcmbank Disease
29065
Itcmdb Generated
ITX-DISEASE-B6A81404E645
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Cavitary Optic Disc Anomalies Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Cavitary Optic Disc Anomalies
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Eye diseases
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
Disease or Syndrome