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DO Term : von Willebrand's disease 2 [DOID:0060574] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A von Willebrand's disease characterized by qualitative but not quantitative abnormalities of the VWF protein that has_material_basis_in mutation in the VWF gene which maps to chromosome 12p13.

synonyms:
von Willebrand disease type II,
613554,
von Willebrand disease type 2,
SNOMEDCT_US_2023_03_01:128107007,
VWD2,
ICD10CM:D68.02,
ORDO:166081,
UMLS_CUI:C1264040,
MESH:D056728,
OMIM:613554,
VWD type 2

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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