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VON WILLEBRAND DISEASES
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DeCS
Descriptor
English
:
von Willebrand Diseases
Descriptor
Spanish
:
Enfermedades de von Willebrand
Descriptor
Portuguese
:
Doenças de von Willebrand
Synonyms
English
:
Angiohemophilia
Hemophilia, Vascular
von Willebrand Disease
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
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
RA
radiography
RI
radionuclide imaging
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
US
ultrasonography
UR
urine
VE
veterinary
VI
virology
Record Number:
15243
Unique Identifier:
D014842
Occurrence in VHL
:
Similar:
DeCS
CID-10
SciELO
LILACS
LIS