Search Ontology:
Human Disease

von Willebrand's disease 1

Term ID
DOID:0060573
Synonyms
  • von Willebrand disease type 1
  • von Willebrand disease type I
  • VWD type 1
  • VWD1
Definition
A von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has_material_basis_in heterozygous mutation in the VWF gene on chromosome 12p13. (2)
References
Ontology
Human Disease   ( DOID:0060573 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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