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About: von Willebrand's disease 1     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

AttributesValues
type
subClassOf
label
  • von Willebrand's disease 1
described by
id
  • DOID:0060573
database_cross_reference
  • MESH:D056725
  • NCI:C131685
  • OMIM:193400
  • SNOMEDCT_US_2021_09_01:128106003
  • UMLS_CUI:C1264039
has_exact_synonym
  • VWD type 1 (en)
  • VWD1 (en)
  • von Willebrand disease type 1 (en)
  • von Willebrand disease type I (en)
has_obo_namespace
  • disease_ontology
in_subset
http://purl.obolib...g/obo/IAO_0000115
  • 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.
is topic of
is annotatedSource of
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