OBO ID: DOID:0060574
Term Name: von Willebrand's disease 2 Search Ontology:
Synonyms:
  • von Willebrand disease type 2
  • von Willebrand disease type II
  • VWD type 2
  • VWD2
Definition: A von Willebrand's disease characterized by qualitative but not quantitative abnormalities of the VWF protein that has_material_basis_in mutation in the VWF gene which maps to chromosome 12p13. https://www.ncbi.nlm.nih.gov/pubmed/20409624
References:
Ontology: Human Disease   ( DOID:0060574 )
Relationships
is a type of:
OTHER von Willebrand's disease 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
VWF von Willebrand disease, types 2A, 2B, 2M, and 2N 613554
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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