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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > alpha 1-Antitrypsin Deficiency
Respiratory Tract Diseases > Lung Diseases > alpha 1-Antitrypsin Deficiency
Digestive System Diseases > Liver Diseases > alpha 1-Antitrypsin Deficiency
Pathological Conditions, Signs and Symptoms > Pathologic Processes > Emphysema > Subcutaneous Emphysema > alpha 1-Antitrypsin Deficiency

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alpha 1-Antitrypsin Deficiency  

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Tipo

  • mesh:Descriptor

Definición

  • Deficiency of the protease inhibitor ALPHA 1-ANTITRYPSIN that manifests primarily as PULMONARY EMPHYSEMA and LIVER CIRRHOSIS.

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URI

http://data.loterre.fr/ark:/67375/JVR-DSQ5R9HN-B

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