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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
platelet-type bleeding disorder 3  
Von Willebrand Disease, X-Linked Form 
Von Willebrand Factor, Deficiency  
von Willebrand's disease 1  
von Willebrand's disease 2  
von Willebrand's disease 3  
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. (DO)

Synonyms
Exact Synonyms: Type 3 VWD ;   Type 3 Von Willebrand's Disease ;   VWD3 ;   Von Willebrand disease III ;   von Willebrand disease type 3 ;   von Willebrand disease type III ;   von Willebrand disease, severe form
Primary IDs: MESH:D056729
Alternate IDs: OMIA:001058 ;   OMIM:277480
Xrefs: ICD10CM:D68.03 ;   NCI:C85213 ;   ORDO:166096
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/19630771 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/3258663 "DO" "DO"

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