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DO Term : von Willebrand's disease 1 [DOID:0060573] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
SNOMEDCT_US_2023_03_01:128106003,
OMIM:193400,
NCI:C131685,
von Willebrand disease type I,
193400,
MESH:D056725,
ICD10CM:D68.01,
VWD type 1,
von Willebrand disease type 1,
UMLS_CUI:C1264039,
VWD1

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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