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Results 41 - 50 of 164 for Anemia
  1. KLF1 gene 
    ... has been identified in people with congenital dyserythropoietic anemia (CDA) type IV. This condition is characterized by ... caused by abnormal red blood cell formation (dyserythropoietic anemia). In people with CDA type IV, immature red ...
    https://medlineplus.gov/genetics/gene/klf1 - Genetics
  2. ABCB7 gene 
    ... been identified in people with X-linked sideroblastic anemia with ataxia. Each of these mutations changes a ... usual role in heme production and iron homeostasis. Anemia results when heme cannot be produced normally, and ...
    https://medlineplus.gov/genetics/gene/abcb7 - Genetics
  3. Glucose-6-phosphate dehydrogenase deficiency 
    ... with glucose-6-phosphate dehydrogenase deficiency is hemolytic anemia, which occurs when red blood cells are destroyed ... the body can replace them. This type of anemia leads to paleness, yellowing of the skin and ...
    https://medlineplus.gov/...cose-6-phosphate-dehydrogenase-deficiency - Genetics
  4. SLC11A2 gene 
    ... gene have been found to cause hypochromic microcytic anemia with iron overload. This condition is characterized by a shortage of red blood cells (anemia) that is apparent at birth. The red blood ...
    https://medlineplus.gov/genetics/gene/slc11a2 - Genetics
  5. RACGAP1 gene 
    ... have been identified in people with congenital dyserythropoietic anemia (CDA) type III. This condition is characterized by ... caused by abnormal red blood cell formation (dyserythropoietic anemia). In people with CDA type III, immature red ...
    https://medlineplus.gov/genetics/gene/racgap1 - Genetics
  6. TERT 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 TERT gene reduce ...
    https://medlineplus.gov/genetics/gene/tert - Genetics
  7. Alpha thalassemia 
    ... also have a shortage of red blood cells (anemia), which can cause pale skin, weakness, fatigue, and ... birth. Additional signs and symptoms can include severe anemia, an enlarged liver and spleen (hepatosplenomegaly), heart defects, ...
    https://medlineplus.gov/genetics/condition/alpha-thalassemia - Genetics
  8. Homocystinuria 
    ... also cause and a blood disorder called megaloblastic anemia, which occurs when a person has a low number of red blood cells (anemia), and the remaining red blood cells are larger ...
    https://medlineplus.gov/genetics/condition/homocystinuria - Genetics
  9. TMPRSS6 gene 
    ... been found to cause an inherited form of anemia called iron-refractory iron deficiency anemia. This condition is characterized by a shortage (deficiency) ...
    https://medlineplus.gov/genetics/gene/tmprss6 - Genetics
  10. ALAS2 gene 
    ... least 50 mutations that cause X-linked sideroblastic anemia have been identified in the ALAS2 gene. Almost ... to the characteristic features of X-linked sideroblastic anemia. More About This Health Condition 5-aminolevulinate synthase, ...
    https://medlineplus.gov/genetics/gene/alas2 - Genetics
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