DiseaseID 12199
血管性血友病3型
disease
NCI2016_02D:The most severe form of von Willebrand disease, inherited in an autosomal recessive pattern. It is characterized by marked deficiency or absence of von Willebrand factor in the plasma and platelets, and low p
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Disease: 1Symptom: 5Target: 1Links: 6
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 12199
- Core Entity Id
- 69683
- Source Entity Count
- 1
- Preferred Name
- Von Willebrand Disease, Type 3
- Name Cn
- 血管性血友病3型
- Name Pinyin
- Xue Guan Xing Xue You Bing 3 Xing
- Name En
- Von Willebrand Disease, Type 3
- 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
- NCI2016_02D:The most severe form of von Willebrand disease, inherited in an autosomal recessive pattern. It is characterized by marked deficiency or absence of von Willebrand factor in the plasma and platelets, and low plasma levels of factor VIII. It may cause severe bleeding.|MSH2017_2016_08_12:A subtype of von Willebrand disease that results from a total or near total 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 3
Role
preferred
Name
VON WILLEBRAND DISEASE, TYPE III
Role
alias
Name
VWD, TYPE 3
Role
alias
Name
VWD3
Role
alias
Name
Von Willebrand'S Disease 3
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS012923
Me Sh
D056729
Omim
277480
Umls
C1264041
Sym Map
SMDE01199
Do Class
DOID:630DOID:7
Dis Ge Net
C1264041
Umls Sty
T047
Me Sh Class
C15C16
Tcmbank Disease
10114
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
NCI2016_02D:The most severe form of von Willebrand disease, inherited in an autosomal recessive pattern. It is characterized by marked deficiency or absence of von Willebrand factor in the plasma and platelets, and low plasma levels of factor VIII. It may cause severe bleeding.|MSH2017_2016_08_12:A subtype of von Willebrand disease that results from a total or near total 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