Hematological, hereditary

Anemia

Arthrogryposis renal dysfuntion and cholestasis

Capillary malformation-arteriovenous malformation

Coagulation factor deficiency

Dyskeratosis congenita

Epstein syndrome

Fechtner syndrome

Fibrinogenemia (a-, hypo-, dys-)

Glanzmann thrombasthenia

Glucocorticoid receptor deficiency

Gray platelet syndrome

Hemostatic/thrombotic disorders (WES)

Hereditary angioedema

Hyper-IgD syndrome

May-Hegglin syndrome

Platelet dysfunction, familial (with AML)

Protein C deficiency

Scott syndrome

Sebastian syndrome

Thrombocytopenia, X-linked

Thrombotic Thrombocytopenic Purpura (TTP)

Von Willebrand disease