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Term:
Parent Terms Term With Siblings Child Terms
blood protein disease +     
agammaglobulinemia +   
Anhaptoglobinemia  
antithrombin III deficiency  
Corticosteroid-Binding Globulin, Elevated 
Deficiency of Plasma Clot Retraction Factor 
dysgammaglobulinemia +   
Hypergammaglobulinemia +   
Hypergastrinemia  
Hypoglobulinemia and Absent B Cells 
Hypoproteinemia +   
Kininogen Deficiency, High Molecular Weight and Low Molecular Weight  
Paraproteinemias +   
protein C deficiency +   
protein S deficiency +   
sickle cell disease +   
A blood protein disease that is characterized by chronic hemolytic anemia and intermittent vaso-occlusive events that result in tissue ischemia leading to acute and chronic pain as well as organ damage that can affect any organ system, resulting from the replacement of one of the beta-globin subunits in hemoglobin with atypical hemoglobin molecules called hemoglobin S which can distort red blood cells into a sickle or crescent shape. Sickle cell disease subtypes should include a detailed genotypic description for the hemoglobin molecules (e.g., Hb S/S, Hb S/C, Hb S/β0-thalassemia). (DO)
sulfhemoglobinemia +  
 sickle cell anemia +