Disease | von willebrand disease |
Phenotype | C0040015|thrombasthenia |
Sentences | 1 |
PubMedID- 24418945 | We report a case of glanzmann thrombasthenia combined with type 2n von willebrand disease (vwd), a variant characterized by an impaired capacity of fviii to bind von willebrand factor (vwf), which results in an autosomally transmitted reduction in circulating fviii levels. |
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