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Results 31 - 40 of 164 for Anemia
  1. RPS10 gene 
    ... have been identified in individuals with Diamond-Blackfan anemia. This disorder primarily affects the bone marrow, which ... The RPS10 gene mutations that cause Diamond-Blackfan anemia are believed to result in an abnormally short, ...
    https://medlineplus.gov/genetics/gene/rps10 - Genetics
  2. RPS17 gene 
    ... have been identified in individuals with Diamond-Blackfan anemia. This disorder primarily affects the bone marrow, which ... The RPS17 gene mutations that cause Diamond-Blackfan anemia are believed to cause problems with ribosomal function. ...
    https://medlineplus.gov/genetics/gene/rps17 - Genetics
  3. RPL5 gene 
    ... have been identified in individuals with Diamond-Blackfan anemia. This disorder primarily affects the bone marrow, which ... The RPL5 gene mutations that cause Diamond-Blackfan anemia are either inherited or occur early in development ...
    https://medlineplus.gov/genetics/gene/rpl5 - Genetics
  4. RPS24 gene 
    ... have been identified in individuals with Diamond-Blackfan anemia. This disorder primarily affects the bone marrow, which ... The RPS24 gene mutations that cause Diamond-Blackfan anemia are believed to cause problems with ribosomal function. ...
    https://medlineplus.gov/genetics/gene/rps24 - Genetics
  5. CDAN1 gene 
    ... have been identified in people with congenital dyserythropoietic anemia (CDA) type I. This condition is characterized by ... caused by abnormal red blood cell formation (dyserythropoietic anemia). In people with CDA type I, immature red ...
    https://medlineplus.gov/genetics/gene/cdan1 - Genetics
  6. RPS19 gene 
    ... have been identified in individuals with Diamond-Blackfan anemia. This disorder primarily affects the bone marrow, which ... The RPS19 gene mutations that cause Diamond-Blackfan anemia are believed to cause problems with ribosomal function. ...
    https://medlineplus.gov/genetics/gene/rps19 - Genetics
  7. CDIN1 gene 
    ... have been identified in people with congenital dyserythropoietic anemia (CDA) type I. This condition is characterized by ... caused by abnormal red blood cell formation (dyserythropoietic anemia). In people with CDA type I, immature red ...
    https://medlineplus.gov/genetics/gene/cdin1 - Genetics
  8. KIF23 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/kif23 - Genetics
  9. TRNT1 deficiency 
    ... TRNT1 deficiency is a blood condition called sideroblastic anemia, which is characterized by a shortage of red blood cells (anemia). In TRNT1 deficiency, the red blood cells that ...
    https://medlineplus.gov/genetics/condition/trnt1-deficiency - Genetics
  10. SEC23B gene 
    ... have been identified in people with congenital dyserythropoietic anemia (CDA) type II.This condition is characterized by ... caused by abnormal red blood cell formation (dyserythropoietic anemia). In people with CDA type II, immature red ...
    https://medlineplus.gov/genetics/gene/sec23b - Genetics
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