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Results 1 - 10 of 36 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. 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
  5. Progressive familial heart block 
    ... impaired cardiac cells over time can lead to fibrosis, worsening the heart block.Mutations in other genes, some of which are unknown, account for the remaining cases of progressive familial heart block. SCN5A TRPM4 Additional Information from NCBI ...
    https://medlineplus.gov/.../progressive-familial-heart-block - Genetics
  6. Hypermanganesemia with dystonia 
    ... HMNDYT Genetic Testing Registry: Hypermanganesemia with dystonia 2 ... Mukhopadhyay S. Familial manganese-induced neurotoxicity due to mutations in SLC30A10 ...
    https://medlineplus.gov/.../hypermanganesemia-with-dystonia - Genetics
  7. North American Indian childhood cirrhosis 
    ... C, Gabbiani G, Morin CL, Roy CC. Severe familial cholestasis in North American Indian children: a clinical model of microfilament dysfunction? Gastroenterology. 1981 Oct;81(4):653-62. Citation on PubMed
    https://medlineplus.gov/...north-american-indian-childhood-cirrhosis - Genetics
  8. Complete plasminogen activator inhibitor 1 deficiency 
    ... deficiency develop scar tissue in the heart (cardiac fibrosis), which can lead to heart failure. Complete PAI-1 deficiency is a rare disorder; its prevalence is unknown. It has been well studied in a large family belonging to the Old Order Amish population of ...
    https://medlineplus.gov/...sminogen-activator-inhibitor-1-deficiency - Genetics
  9. Congenital fibrosis of the extraocular muscles 
    ... CFEOM1 is the most common form of congenital fibrosis of the extraocular muscles, affecting at least 1 in 230,000 people. CFEOM1 and CFEOM3 have been reported worldwide, whereas CFEOM2 has been seen in only a few families of Turkish, Saudi Arabian, and Iranian descent. Tukel ...
    https://medlineplus.gov/...nital-fibrosis-of-the-extraocular-muscles - Genetics
  10. Sick sinus syndrome 
    ... node may harden and develop scar-like damage (fibrosis) that prevents it from working properly. ... which means they occur in people with no history of the disorder in their family.When sick sinus syndrome results from mutations in ...
    https://medlineplus.gov/genetics/condition/sick-sinus-syndrome - Genetics
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