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VON WILLEBRAND DISEASE
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DeCS
Descriptor
English
:
von Willebrand Disease
Descriptor
Spanish
:
Enfermedad de von Willebrand
Descriptor
Portuguese
:
Doença de von Willebrand
Synonyms
English
:
Angiohemophilia
Hemophilia, Vascular
Tree Number:
C15.378.100.100.900
C15.378.100.141.900
C15.378.140.900
C15.378.463.920
C16.320.099.900
Definition
English
:
Group of
hemorrhagic disorders
in which the
von Willebrand factor
(Factor VIII-related antigen) 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
:
do not coord with
INFANT
, NEWBORN, DISEASES
History Note
English
:
99(63)
Allowable Qualifiers
English
:
blood
cerebrospinal fluid
chemically induced
classification
complications
diet therapy
diagnosis
drug therapy
economics
ethnology
embryology
enzymology
epidemiology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
pathology
prevention & control
physiopathology
parasitology
psychology
radiography
rehabilitation
radionuclide imaging
radiotherapy
surgery
therapy
urine
ultrasonography
veterinary
virology
Record Number:
15243
Unique Identifier:
D014842
Occurrence in VHL
:
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