DiseaseID 12198
血管性血友病2型
disease
MSH2017_2016_08_12:A subtype of von Willebrand disease that results from qualitative deficiencies of VON WILLEBRAND FACTOR. The subtype is divided into several variants with each variant having a distinctive pattern of P
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Disease: 1Symptom: 3Target: 1Links: 4
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 12198
- Core Entity Id
- 69682
- Source Entity Count
- 1
- Preferred Name
- Von Willebrand Disease, Type 2
- Name Cn
- 血管性血友病2型
- Name Pinyin
- Xue Guan Xing Xue You Bing 2 Xing
- Name En
- Von Willebrand Disease, Type 2
- 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 qualitative deficiencies of VON WILLEBRAND FACTOR. The subtype is divided into several variants with each variant having a distinctive pattern of PLATELET-interaction.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Von Willebrand Disease, Type 2
Role
preferred
Name
Von Willebrand Disease Type 2M
Role
preferred
Name
Von Willebrand Disease, Type 2A
Role
preferred
Name
Von Willebrand Disease, Type 2B
Role
preferred
Name
Von Willebrand Disease, Type 2N
Role
preferred
Name
VON WILLEBRAND FACTOR VICENZA PHENOTYPE
Role
preferred
Name
Type 2M Von Willebrand Disease
Role
alias
Name
VON WILLEBRAND DISEASE, TYPE 2M
Role
alias
Name
VON WILLEBRAND DISEASE, TYPE II
Role
alias
Name
VWD, TYPE 2
Role
alias
Name
VWD2
Role
alias
Name
VWD2A
Role
alias
Name
VWD2B
Role
alias
Name
VWD2M
Role
alias
Name
VWD2N
Role
alias
Name
Von Willebrand Factor Vicenza
Role
alias
Name
Von Willebrand'S Disease 2
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS012922HBDIS013194HBDIS013195HBDIS013196HBDIS013197HBDIS023461
Me Sh
D056728
Omim
613554
Umls
C1264040C1282968C1282971C1282974C1282975
Sym Map
SMDE02199SMDE14327SMDE14328SMDE14329SMDE14330
Do Class
DOID:630DOID:7
Dis Ge Net
C1264040C1282968C1282971C1282974C1282975C4017650
Umls Sty
T033T047
Me Sh Class
C15C16
Tcmbank Disease
1000013467164572887299649330
Itcmdb Generated
ITX-DISEASE-F11B8C9753AB
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
0
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
diseasephenotype
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or SyndromeFinding
Disease Definition
MSH2017_2016_08_12:A subtype of von Willebrand disease that results from qualitative deficiencies of VON WILLEBRAND FACTOR. The subtype is divided into several variants with each variant having a distinctive pattern of PLATELET-interaction.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or SyndromeFinding