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Metadata
ID DOID:0111054
Name von Willebrand's disease 3
Definition A von Willebrand's disease characterized by autosomal recessive inheritance of a severe quantitative defect or virtual absence of VWF in plasma, prolonged bleeding time, and more severe bleeding tendencies compared to the other types of von Willebrand disease that has material_basis_in homozygous or compound heterozygous mutation in the VWF gene which maps to chromosome 12p13.
https://www.ncbi.nlm.nih.gov/pubmed/19630771, https://www.ncbi.nlm.nih.gov/pubmed/3258663
Xrefs

MESH:D056729

NCI:C85213

OMIM:277480

ORDO:166096

UMLS_CUI:C1264041

Subsets

NCIthesaurus

Synonyms

von Willebrand disease type 3 [EXACT]

von Willebrand disease type III [EXACT]

VWD type 3 [EXACT]

VWD3 [EXACT]

Parent Relationships

is_a von Willebrand's disease

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