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Results 1 - 10 of 65 for "Cirrhosis," familial
  1. Cryptogenic cirrhosis 
    ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov CIRRHOSIS, FAMILIAL PubMed Caldwell S. Cryptogenic cirrhosis: what are we missing? Curr Gastroenterol Rep. 2010 ...
    https://medlineplus.gov/genetics/condition/cryptogenic-cirrhosis - Genetics
  2. Hereditary hemochromatosis 
    ... one parent with the condition. Bronze diabetes Bronzed cirrhosis Familial hemochromatosis Genetic hemochromatosis Haemochromatosis HC Hemochromatosis Hereditary haemochromatosis ...
    https://medlineplus.gov/.../condition/hereditary-hemochromatosis - Genetics
  3. Retroperitoneal fibrosis 
    ... Goldstein H, Kessler B, Vinocur C, Marchildon MB. Familial retroperitoneal fibrosis. J Pediatr Surg. 1987 Dec;22(12):1092- ...
    https://medlineplus.gov/genetics/condition/retroperitoneal-fibrosis - Genetics
  4. CFTR gene 
    ... cAMP-dependent chloride channel CF CFTR_HUMAN cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) cystic fibrosis transmembrane conductance regulator, ...
    https://medlineplus.gov/genetics/gene/cftr - Genetics
  5. Idiopathic pulmonary fibrosis 
    ... a small percentage of cases of idiopathic pulmonary fibrosis appear to run in families. The cause of idiopathic pulmonary fibrosis is unknown. ... in about 15 percent of all cases of familial pulmonary fibrosis and a smaller percentage of cases of sporadic ...
    https://medlineplus.gov/.../condition/idiopathic-pulmonary-fibrosis - Genetics
  6. TERC gene 
    ... been found in cases that run in families (familial pulmonary fibrosis) and, less commonly, in isolated (sporadic) cases. Some individuals with idiopathic pulmonary fibrosis due to TERC gene mutations have family members with other features of dyskeratosis congenita (described ...
    https://medlineplus.gov/genetics/gene/terc - Genetics
  7. TERT gene 
    ... been found in cases that run in families (familial pulmonary fibrosis) and, less commonly, in isolated (sporadic) cases. Some individuals with idiopathic pulmonary fibrosis due to TERT gene mutations have family members with other features of dyskeratosis congenita (described ...
    https://medlineplus.gov/genetics/gene/tert - Genetics
  8. What are the different ways a genetic condition can be inherited?: MedlinePlus Genetics 
    ... not seen in every generation of an affected family. cystic fibrosis , sickle cell disease X-linked dominant X-linked ...
    https://medlineplus.gov/.../inheritance/inheritancepatterns - Genetics
  9. PHOX2A gene 
    ... A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2). Am J ...
    https://medlineplus.gov/genetics/gene/phox2a - Genetics
  10. Why is it important to know my family health history?: MedlinePlus Genetics 
    ... mutations) in a single gene, such as cystic fibrosis and sickle cell disease . While a family health history provides information about the risk of ...
    https://medlineplus.gov/.../understanding/inheritance/familyhistory - Genetics
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