DiseaseID 12197
血管性血友病1型
disease
MSH2017_2016_08_12:A subtype of von Willebrand disease that results from a partial deficiency of VON WILLEBRAND FACTOR.
Relationship Network
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Disease: 1Symptom: 4Target: 5Links: 9
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 12197
- Core Entity Id
- 69681
- Source Entity Count
- 1
- Preferred Name
- Von Willebrand Disease, Type 1
- Name Cn
- 血管性血友病1型
- Name Pinyin
- Xue Guan Xing Xue You Bing 1 Xing
- Name En
- Von Willebrand Disease, Type 1
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:A subtype of von Willebrand disease that results from a partial deficiency of VON WILLEBRAND FACTOR.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Von Willebrand Disease, Type 1
Role
preferred
Name
VON WILLEBRAND DISEASE, TYPE I
Role
alias
Name
VWD, TYPE 1
Role
alias
Name
VWD1
Role
alias
Name
Von Willebrand'S Disease 1
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS012921
Me Sh
D056725
Omim
193400
Umls
C1264039
Sym Map
SMDE02982
Do Class
DOID:630DOID:7
Dis Ge Net
C1264039
Umls Sty
T047
Me Sh Class
C15C16
Tcmbank Disease
1438
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Disease Definition
MSH2017_2016_08_12:A subtype of von Willebrand disease that results from a partial deficiency of VON WILLEBRAND FACTOR.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome