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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
Pathological Conditions, Signs and Symptoms > Pathologic Processes > Emphysema > Subcutaneous Emphysema > alpha 1-Antitrypsin Deficiency
Digestive System Diseases > Liver Diseases > alpha 1-Antitrypsin Deficiency

Preferred term

alpha 1-Antitrypsin Deficiency  

Type

  • Topical Descriptor

Broader concept

Related concepts

Note

  • Pi or PiZZ goes here + PHENOTYPE

Scope note

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

History note

  • 98

In other languages

URI

http://www.yso.fi/onto/mesh/D019896

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