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| Term | von Willebrand's disease | ID (Ontology) | DOID:12531 (Human Disease) |
| Definition | 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. | ||
| Also Known As | "vascular hemophilia" ; "vascular pseudohemophilia" ; "von Willebrand disease" (for all, see Synonyms field below) | ||
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blood coagulation disease |__hemophilia |__von Willebrand's disease 1 rec. |__von Willebrand's disease 1 1 rec. |__von Willebrand's disease 2 1 rec. |__von Willebrand's disease 3 1 rec. |
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| Is a | hemophilia | ||
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GARD:7867 ICD10CM:D68.0 ICD9CM:286.4 MESH:D014842 NCI:C68677 SNOMEDCT_US_2023_03_01:11093006 UMLS_CUI:C0042974 |
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