| HNSHA | hereditary nonspherocytic hemolytic anemia |
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| HU | heat unit; hemagglutinating unit; hemolytic unit; Hounsfield unit; human urine, human urinary; hydro... |
| HUS | hemolytic uremic syndrome; hyaluronidase unit for semen |
| IAHA | idiopathic autoimmune hemolytic anemia; immune adherence hemagglutination |
| IAHD | idiopathic acquired hemolytic disorder |
| hemolytic disease of the newborn |
Neonatal disease characterized by anemia, jaundice, liver and spleen enlargement, and generalized edema (hydrops fetalis). SYN: erythroblastosis fetalis. SEE: Rh blood group.
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| hemolytic icterus |
Hemolytic jaundice.
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| hemolytic unit |
The amount of inactivated immune serum that causes complete hemolysis of 1 ml of a 5% emulsion of washed red blood cells in the presence of complement.
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| hemolytic anemia |
Anemia that results when red blood cells break open
출처: www2.gsu.edu/~wwwfsm/vocabulary/all_modules.htm
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| hemolytic crisis |
Hemolytic crises are quite rare and usually occur in patients who have glucose-6-phosphate dehydrogenase (G-6-PD) deficiency with sickle cell anemia. It probably results from complications of sickle cell anemia, such as infection, rather than from the disorder itself. Hemolytic crisis causes liver congestion and hepatomegaly as a result of degenerative changes. It worsens chronic jaundice although increased jaundice doesn't always point to a hemolytic crisis.
출처: www.io.com/~hcexres/tcm1603/acchtml/def_ex.html
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