Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 5Target: 1Links: 6
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 12337
- Core Entity Id
- 69834
- Source Entity Count
- 1
- Preferred Name
- Urban Schosser Spohn Syndrome
- Name Cn
- Urban-Schosser-Spohn综合征
- Name Pinyin
- Urban-schosser-spohn Zong He Zheng
- Name En
- Urban Schosser Spohn Syndrome
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms
- Do Class
- Hpo Class
- Mesh Class Name
- Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; 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
Urban Schosser Spohn Syndrome
Role
preferred
Name
Mucoepithelial Dysplasia, Hereditary
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS013075
Omim
158310
Umls
C1274795
Sym Map
SMDE14102
Dis Ge Net
C1274795
Umls Sty
T019
Me Sh Class
C16C17C23
Tcmbank Disease
2832
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Congenital Abnormality
Me Sh Disease Class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Umls Semantic Type Name
Congenital Abnormality