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DO Term : von Willebrand's disease [DOID:12531] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hemophilia that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion.

synonyms:
ICD9CM:286.4,
NCI:C68677,
vascular pseudohemophilia,
von Willebrand disease,
ICD10CM:D68.0,
GARD:7867,
UMLS_CUI:C0042974,
SNOMEDCT_US_2023_03_01:11093006,
MESH:D014842,
vascular hemophilia,
von Willebrand disorder,
von Willebrand-Jrgens disease,
von Willebrand's-Jurgens' disease

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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