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  2. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Two cases of von Willebrand disease type 3 in consanguineous Chinese families
    1
    1. ClingenBaseline 21 Oct 2026
      in Baseline Annotations
      Two cases of von Willebrand disease type 3 in consanguineousChinese families

      PMID: 31793247

      Gene: VMF

      HGNCID: HGNC:12726

      General HGNC:VWF inferred_gene_hgnc:12726 inferred_gene_source:HGNC_body ClinGen VWF
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    • General
    • inferred_gene_source:HGNC_body
    • HGNC:VWF
    • inferred_gene_hgnc:12726
    • ClinGen VWF

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    • ClingenBaseline

    URL

    pmc.ncbi.nlm.nih.gov/articles/PMC7005608/pdf/MGG3-8-e1075.pdf
  3. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    A Homozygous Deep Intronic Variant Causes Von Willebrand Factor Deficiency and Lack of Endothelial-Specific Secretory Organelles, Weibel–Palade Bodies
    1
    1. ClingenBaseline 21 Oct 2026
      in Baseline Annotations
      A Homozygous Deep Intronic Variant Causes Von Willebrand Factor Deficiency and Lack of Endothelial-Specific Secretory Organelles, Weibel–Palade Bodies

      PMID: 35328514 Gene: VWF HGNCID: HGNC:12726

      General HGNC:VWF inferred_gene_hgnc:12726 inferred_gene_source:HGNC_body ClinGen VWF
    Visit annotations in context

    Tags

    • General
    • inferred_gene_source:HGNC_body
    • HGNC:VWF
    • inferred_gene_hgnc:12726
    • ClinGen VWF

    Annotators

    • ClingenBaseline

    URL

    pmc.ncbi.nlm.nih.gov/articles/PMC8950443/
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