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Results 51 - 60 of 164 for Anemia
  1. SLC19A2 gene 
    ... have been found to cause thiamine-responsive megaloblastic anemia syndrome, also called TRMA. TRMA is a rare ... loss, diabetes, and a blood disorder called megaloblastic anemia. TRMA is called "thiamine-responsive" because the anemia ...
    https://medlineplus.gov/genetics/gene/slc19a2 - Genetics
  2. GATA1 gene 
    ... GATA1 gene have been found to cause dyserythropoietic anemia and thrombocytopenia. Most of these mutations change a ... differentiation causes a shortage of red blood cells (anemia) and platelets involved in blood clotting (thrombocytopenia), which ...
    https://medlineplus.gov/genetics/gene/gata1 - Genetics
  3. Glutathione synthetase deficiency 
    ... in the destruction of red blood cells (hemolytic anemia). In addition, affected individuals may release large amounts ... experience symptoms beginning shortly after birth including hemolytic anemia, 5-oxoprolinuria, and elevated acidity in the blood ...
    https://medlineplus.gov/.../glutathione-synthetase-deficiency - Genetics
  4. Atypical hemolytic-uremic syndrome 
    ... three major features related to abnormal clotting: hemolytic anemia, thrombocytopenia, and kidney failure.Hemolytic anemia occurs when red blood cells break down (undergo ...
    https://medlineplus.gov/.../atypical-hemolytic-uremic-syndrome - Genetics
  5. SLC4A1 gene 
    ... The blood cell abnormalities can lead to hemolytic anemia, in which the abnormal red blood cells are ... abnormal red blood cells may lead to hemolytic anemia. More About This Health Condition Mutations in the ...
    https://medlineplus.gov/genetics/gene/slc4a1 - Genetics
  6. Sitosterolemia 
    ... resulting in a shortage of red blood cells (anemia). This type of anemia is called hemolytic anemia. Affected individuals sometimes have abnormally shaped red blood ...
    https://medlineplus.gov/genetics/condition/sitosterolemia - Genetics
  7. HBA2 gene 
    ... hydrops fetalis), a shortage of red blood cells (anemia), and an enlarged liver and spleen (hepatosplenomegaly). HbH ... HbH disease is characterized by mild to moderate anemia, hepatosplenomegaly, and yellowing of the eyes and skin ( ...
    https://medlineplus.gov/genetics/gene/hba2 - Genetics
  8. Paroxysmal nocturnal hemoglobinuria 
    ... shortage of these cells in the blood (hemolytic anemia), which can cause signs and symptoms such as ... been treated for another blood disease called aplastic anemia may develop PNH. In a small number of ...
    https://medlineplus.gov/.../paroxysmal-nocturnal-hemoglobinuria - Genetics
  9. REN-related kidney disease 
    ... disease develop a shortage of red blood cells (anemia), which can cause pale skin, weakness, and fatigue. In this disorder, anemia is usually mild and begins to improve during ...
    https://medlineplus.gov/.../condition/ren-related-kidney-disease - Genetics
  10. TERC gene 
    ... individuals also develop a serious condition called aplastic anemia, also known as bone marrow failure, which occurs ... of dyskeratosis congenita (described above), such as aplastic anemia or cancer.Mutations in the TERC gene reduce ...
    https://medlineplus.gov/genetics/gene/terc - Genetics
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