Disease Index

human disease

placenta disease that is characterized by insufficient blood flow to the placenta during pregnancy

human disease

specific contagious and frequently fatal human disease caused by Yersinia pestis

non-malignant thickening of the feet's deep connective tissue

human disease

human disease

human disease

type of large B-cell lymphoma

plasma cell dyscrasia in which a plasma cell tumour grows within soft tissue or within the axial skeleton

disorder in which branching casts of the airways are expectorated

Human disease

human disease

Human disease

human disease

human disease

human disease

inherited blood coagulation disease characterized by enhanced binding of von Willebrand factor by the platelet glycoprotein Ib receptor complex that has material basis in mutation in the GP1BA gene on chromosome 17p13.2

Human disease

inherited blood coagulation disease characterized by autosomal dominant inheritance of mild thrombocytopenia, mild alpha-granue deficiency, defective platelet adhesion that has material basis in mutation in the ITGA2 gene on chromosome 5q11.2

although generally lethal, survival to adulthood has been reported in two families

gastrointestinal benign neoplasm that is a located in the salivary glands

Human disease

Human disease

human disease

Human disease

accumulation of pus in the pleural cavity that can develop when bacteria invade it

pulmonary blastoma that derives from the lung or pleural cavity

pleuropulmonary blastoma composed of malignant small cells. Sarcomatous features are absent