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Results 1 - 7 of 7 for "Alpha-1" antitrypsin deficiency
  1. Alpha-1 antitrypsin deficiency is an inherited disorder that may cause lung disease and liver disease. The signs and symptoms of the condition and the age ...
  2. ... gene have been associated with a condition called alpha-1 antitrypsin deficiency. This condition is characterized by a shortage (deficiency) ... s structure. The most common variant that causes alpha-1 antitrypsin deficiency replaces the amino acid glutamic acid with the ...
  3. ... biochemical defect that causes the condition (for example, alpha-1 antitrypsin deficiency ); The gene in which the variant (or mutation) ...
  4. ... characteristics of the genetic condition. ABO blood group, alpha-1 antitrypsin deficiency Mitochondrial Mitochondrial inheritance , also known as maternal inheritance, ...
  5. ... including MUTYH-associated polyposis Age-related macular degeneration Alpha-1 antitrypsin deficiency Celiac disease Familial hypercholesterolemia Glucose-6-phosphate dehydrogenase ...
  6. ... gene in each cell. Like thyroxine-binding globulin deficiency, thyroxine-binding globulin excess does not cause any problems with thyroid function. alpha-1 antiproteinase, antitrypsin serine (or cysteine) proteinase inhibitor, clade A (alpha- ...
  7. ... globulin serine (or cysteine) proteinase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6 serpin A6 serpin peptidase inhibitor, clade ...