Search on: HEMOPHILIA, VASCULAR 
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Descriptor English:   von Willebrand Diseases 
Descriptor Spanish:   Enfermedades de von Willebrand 
Descriptor Portuguese:   Doenças de von Willebrand 
Synonyms English:   Angiohemophilia
Angiohemophilias
Disorder, Von Willebrand
Hemophilia, Vascular
Pseudohemophilia, Vascular
Pseudohemophilias, Vascular
Vascular Hemophilia
Vascular Hemophilias
Vascular Pseudohemophilia
Vascular Pseudohemophilias
Von Willebrand Disorder
Von Willebrand's Factor Deficiency
von Willebrand Disease
von Willebrand Disease, Recessive Form
von Willebrand's Disease
von Willebrand's Diseases  
Tree Number:   C15.378.100.100.900
C15.378.100.141.900
C15.378.140.900
C15.378.463.920
C16.320.099.920
Definition English:   Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion. 
Indexing Annotation English:   note specific types of Von Willebrand Disease are available
History Note English:   2010(1963) 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   15243 
Unique Identifier:   D014842 

Occurrence in VHL:
 
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