JSON

von Willebrand's disease 1

Go to external page http://purl.obolibrary.org/obo/DOID_0060573

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. [ http://purl.obolibrary.org/obo/ECO_0007645 url:https://www.ncbi.nlm.nih.gov/pubmed/16889557 url:https://www.ncbi.nlm.nih.gov/pubmed/8456432 ]

Synonyms: von Willebrand disease type I VWD1 von Willebrand disease type 1 VWD type 1

This is just here as a test because I lose it

Term information

database cross reference
  • SNOMEDCT_US_2023_03_01:128106003
  • MIM:193400
  • MESH:D056725
  • ICD10CM:D68.01
  • NCI:C131685
  • UMLS_CUI:C1264039
Subsets

NCIthesaurus

acronym
VWD1

has obo namespace

disease_ontology

id

DOID:0060573

Term relations