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".ALPHA.1-PROTEINASE" INHIBITOR HUMAN
- Learning about Alpha-1 Antitrypsin Deficiency (AATD) (National Human Genome Research Institute)National Human Genome Research Institute
- Hemochromatosis (American Liver Foundation)Hemochromatosis/Start Here ... Hemochromatosis ... Hemochromatosis is an inherited condition in which the body absorbs and stores too much iron in the skin, heart, ...
- Galactosemia (American Liver Foundation)Carbohydrate Metabolism Disorders/Specifics ... Carbohydrate Metabolism Disorders ... Liver Diseases/Children ... Liver Diseases ... Galactosemia is an inherited disorder ...
- Glycogen Storage Disease Type 1 (von Gierke) (American Liver Foundation)Carbohydrate Metabolism Disorders/Specifics ... Carbohydrate Metabolism Disorders ... Liver Diseases/Children ... Liver Diseases ... American Liver Foundation ... Type I glycogen ...
- Alagille Syndrome (American Liver Foundation)Liver Diseases/Children ... Liver Diseases ... American Liver Foundation ... Alagille Syndrome is an inherited disorder that closely resembles other forms of liver disease ...
- Benign Liver Tumors (American Liver Foundation)Liver Diseases/Specifics ... Liver Diseases ... Benign Tumors/Specifics ... Benign Tumors ... American Liver Foundation ... There are 3 main types of benign liver tumors. They ...
- Primary Sclerosing Cholangitis (PSC) (American Liver Foundation)Liver Diseases/Specifics ... Liver Diseases ... Bile Duct Diseases/Specifics ... Bile Duct Diseases ... American Liver Foundation ... Primary sclerosing cholangitis (PSC) is a ...