OBO ID: DOID:0060573
Term Name: von Willebrand's disease 1 Search Ontology:
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 von Willebrand's disease 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
VWF von Willebrand disease, type 1 193400
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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