"SNOMEDCT_US_2021_09_01:51720005"^^ . _:vb50944125 . _:vb50944124 . _:vb50944124 . _:vb50944125 . _:vb50944124 . _:vb50944124 . . "NCI:C84741"^^ . "UMLS_CUI:C0272302"^^ . "disease_ontology"^^ . "platelet-type bleeding disorder 17"^^ . _:vb50944125 . "DOID:0111049"^^ . "BDPLT17"@en . "OMIM:187900"^^ . "hereditary thrombasthenia-thrombocytopenia"@en . "A blood platelet disease characterized by autosomal dominant inheritance of increased bleeding tendency, gray platelets, thrombocytopenia, thrombasthenia, abnormal megakaryocytes, decreased or absent alpha-granules in platelets, and myelofibrosis that has_material_basis_in heterozygous mutation in the GFI1B gene on chromosome 9q34."^^ . . _:vb50944124 . "ICD10CM:D69.1"^^ . _:vb50944125 . . . _:vb50944125 . "MESH:D055652"^^ . .