Disease | von willebrand disease |
Phenotype | C0040015|glanzmann thrombasthenia |
Sentences | 2 |
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. |
PubMedID- 20147343 | Coinheritance of severe von willebrand disease with glanzmann thrombasthenia. |
Page: 1