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Results 81 - 90 of 164 for Anemia
  1. TRNT1 gene 
    ... Features can include a blood disorder called sideroblastic anemia, recurrent fevers, a shortage of immune cells called ... Fleming MD. Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD). Blood. ...
    https://medlineplus.gov/genetics/gene/trnt1 - Genetics
  2. Aceruloplasminemia 
    ... leading to a shortage of red blood cells (anemia). Anemia and diabetes usually occur by the time an ...
    https://medlineplus.gov/genetics/condition/aceruloplasminemia - Genetics
  3. Warsaw breakage syndrome 
    ... H, de Winter JP. Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome. Anemia. 2010;2010:565268. doi: 10.1155/2010/565268. ...
    https://medlineplus.gov/genetics/condition/warsaw-breakage-syndrome - Genetics
  4. Autoimmune lymphoproliferative syndrome 
    ... system may attack red blood cells (autoimmune hemolytic anemia), white blood cells (autoimmune neutropenia), or platelets (autoimmune ... later, most frequently as a combination of hemolytic anemia and thrombocytopenia, also called Evans syndrome. People with ...
    https://medlineplus.gov/.../autoimmune-lymphoproliferative-syndrome - Genetics
  5. Glycogen storage disease type VII 
    ... hemolytic form of GSDVII is characterized by hemolytic anemia, in which red blood cells are broken down ( ... prematurely, causing a shortage of red blood cells (anemia). People with the hemolytic form of GSDVII do ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-vii - Genetics
  6. Osteopetrosis 
    ... abnormal bleeding, a shortage of red blood cells (anemia), and recurrent infections. In the most severe cases, ... include an increased risk of bone fracture and anemia. People with this form of the disorder typically ...
    https://medlineplus.gov/genetics/condition/osteopetrosis - Genetics
  7. Porphyria 
    ... include a low number of red blood cells (anemia) and enlargement of the spleen (splenomegaly). The other ... function and cause X-linked dominant protoporphyria without anemia or iron overload. Am J Hum Genet. 2008 ...
    https://medlineplus.gov/genetics/condition/porphyria -
  8. HFE gene 
    ... of the iron overload in X-linked sideroblastic anemia when it is inherited along with a mutation ... severe signs and symptoms of X-linked sideroblastic anemia by further increasing the absorption of dietary iron, ...
    https://medlineplus.gov/genetics/gene/hfe - Genetics
  9. AMN gene 
    ... leads to a blood disorder known as megaloblastic anemia. About half of affected individuals also have excess ... development of red blood cells, leading to megaloblastic anemia. Low levels of vitamin B12 can also affect ...
    https://medlineplus.gov/genetics/gene/amn - Genetics
  10. RPS14 gene 
    ... often have a shortage of red blood cells (anemia) and abnormalities in blood cells called megakaryocytes, which ... forming cells in the bone marrow, resulting in anemia. Research suggests that the other features of the ...
    https://medlineplus.gov/genetics/gene/rps14 - Genetics
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