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Results 1 - 10 of 30 for Liver "disease," severe congenital
  1. Factor X deficiency 
    ... factor X deficiency, is more common than the congenital form. Acquired factor X deficiency can be caused by other disorders such as severe liver disease or systemic amyloidosis, a condition involving the accumulation ...
    https://medlineplus.gov/genetics/condition/factor-x-deficiency - Genetics
  2. Microvillus inclusion disease 
    ... and bile salt export pump contribute to cholestatic liver disorder in ... severe congenital enterocyte disorder. J Pediatr Gastroenterol Nutr. 2011 Apr; ...
    https://medlineplus.gov/.../condition/microvillus-inclusion-disease - Genetics
  3. Heterotaxy syndrome 
    ... most serious complications are generally caused by critical congenital heart disease, a group of complex heart defects that are present from birth. Biliary atresia, a problem with the bile ducts in the liver, can also cause severe health problems in infancy.The severity of heterotaxy ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  4. Severe congenital neutropenia 
    Severe congenital neutropenia is a condition that increases the risk of repeated infections in affected individuals. People with this condition have an abnormally ...
    https://medlineplus.gov/.../condition/severe-congenital-neutropenia - Genetics
  5. Factor XI deficiency 
    ... deficiency can also occur as the result of severe liver disease or receiving a transplanted liver from an affected individual. In addition, approximately 25 percent of people with another disorder called Noonan syndrome have factor XI deficiency. F11 Severe factor XI deficiency is passed down in an ...
    https://medlineplus.gov/genetics/condition/factor-xi-deficiency - Genetics
  6. Glycogen storage disease type IV 
    ... features as the progressive hepatic type, but the liver disease is not as severe. In the non-progressive hepatic type, hepatomegaly and liver disease are usually evident in early childhood, but affected ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iv - Genetics
  7. GNE gene 
    ... Study Group. Mutation in GNE is associated with severe congenital thrombocytopenia. Blood. 2018 Oct 25;132(17):1855- ...
    https://medlineplus.gov/genetics/gene/gne - Genetics
  8. Factor VII deficiency 
    ... factor VII deficiency, is less common than the congenital form. It can be caused by liver disease or by blood cell disorders such as myeloma or aplastic anemia. Acquired factor VII deficiency can also be caused by certain drugs such as medicines that prevent clotting, or by a ... Congenital factor VII deficiency is inherited in an autosomal ...
    https://medlineplus.gov/genetics/condition/factor-vii-deficiency - Genetics
  9. X-linked sideroblastic anemia 
    ... a rapid heartbeat, pale skin, and an enlarged liver and spleen (hepatosplenomegaly). Over time, severe medical problems such as heart disease and liver damage (cirrhosis) can result from the ...
    https://medlineplus.gov/.../condition/x-linked-sideroblastic-anemia - Genetics
  10. Congenital generalized lipodystrophy 
    ... lower part of the stomach (pyloric stenosis), and severe arrhythmia that can lead to sudden death. Congenital generalized lipodystrophy has an estimated prevalence of 1 ...
    https://medlineplus.gov/.../congenital-generalized-lipodystrophy - Genetics
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