Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 8Target: 12Links: 20
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 17503
- Core Entity Id
- 75745
- Source Entity Count
- 1
- Preferred Name
- Chromosome 17 Deletion
- Name Cn
- 17号染色体缺失
- Name Pinyin
- 17 Hao Ran Se Ti Que Shi
- Name En
- Chromosome 17 Deletion
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Cell or Molecular Dysfunction
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
- Do Class
- Hpo Class
- Mesh Class Name
- Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System 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
Chromosome 17 Deletion
Role
preferred
Name
Chromosome 17P Deletion Syndrome
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS020336HBDIS022007
Umls
C3683846
Sym Map
SMDE07123
Dis Ge Net
C2931713C3683846
Umls Sty
T049
Me Sh Class
C10C16C23
Tcmbank Disease
17984298
Itcmdb Generated
ITX-DISEASE-58865EBFA923
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
diseasephenotype
Umls Disease Type
Cell or Molecular Dysfunction
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Umls Semantic Type Name
Cell or Molecular Dysfunction