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Results 21 - 30 of 164 for Anemia
  1. FANCC gene 
    ... involved in a process known as the Fanconi anemia (FA) pathway. The FA pathway turns on (activates) ... proteins (including FANCC) and two proteins called Fanconi anemia-associated proteins (FAAPs). This complex activates two proteins, ...
    https://medlineplus.gov/genetics/gene/fancc - Genetics
  2. HBB gene 
    ... fatigue. More About This Health Condition Sickle cell anemia (also called homozygous sickle cell disease or HbSS ... lead to a shortage of red blood cells (anemia). The rigid sickle-shaped cells can block small ...
    https://medlineplus.gov/genetics/gene/hbb - Genetics
  3. SLC4A1-associated distal renal tubular acidosis 
    ... from no symptoms to a condition called hemolytic anemia, in which red blood cells prematurely break down ( ... hemolysis), causing a shortage of red blood cells (anemia). Hemolytic anemia can lead to unusually pale skin ( ...
    https://medlineplus.gov/...-associated-distal-renal-tubular-acidosis - Genetics
  4. 5q minus syndrome 
    ... affected, leading to a shortage of these cells (anemia). In addition, the red blood cells that are ... with 5q- syndrome have no symptoms related to anemia, especially in the early stages of the condition, ...
    https://medlineplus.gov/genetics/condition/5q-minus-syndrome - Genetics
  5. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome 
    ... individuals have low levels of red blood cells (anemia), platelets (thrombocytopenia), or certain white blood cells (neutropenia) ... infection syndrome, X-linked Enteropathy, autoimmune, with hemolytic anemia and polyendocrinopathy IDDM-secretory diarrhea syndrome Immunodeficiency, polyendocrinopathy, ...
    https://medlineplus.gov/...ocrinopathy-enteropathy-x-linked-syndrome - Genetics
  6. MTRR gene 
    The MTRR gene provides instructions for making an enzyme called methionine synthase reductase. This enzyme is required for the proper function of another ...
    https://medlineplus.gov/genetics/gene/mtrr - Genetics
  7. RPS26 gene 
    ... have been identified in individuals with Diamond-Blackfan anemia. This disorder primarily affects the bone marrow, which ... The RPS26 gene mutations that cause Diamond-Blackfan anemia are believed to cause problems with ribosomal function. ...
    https://medlineplus.gov/genetics/gene/rps26 - Genetics
  8. RPL11 gene 
    ... have been identified in individuals with Diamond-Blackfan anemia. This disorder primarily affects the bone marrow, which ... The RPL11 gene mutations that cause Diamond-Blackfan anemia are believed to cause problems with ribosomal function. ...
    https://medlineplus.gov/genetics/gene/rpl11 - Genetics
  9. RPL35A gene 
    ... have been identified in individuals with Diamond-Blackfan anemia. This disorder primarily affects the bone marrow, which ... The RPL35A gene mutations that cause Diamond-Blackfan anemia are believed to cause problems with ribosomal function. ...
    https://medlineplus.gov/genetics/gene/rpl35a - Genetics
  10. GPI gene 
    ... disorder have a condition known as chronic hemolytic anemia, in which red blood cells are broken down ( ... resulting in a shortage of red blood cells (anemia). Some affected individuals also have neurological problems, including ...
    https://medlineplus.gov/genetics/gene/gpi - Genetics
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