A A A+ A- A0 A1 A2 A3 A4 A5 A6 A7 A8 A9 AA AB AC AD AE AF AG AH AI AJ AK AL AM AN AO AP AQ AR AS AT AU AV AW AX AY AZ
alpha 1 antitrypsin deficiency
[autosomal recessive trait leading to destruction of lung tissue by neutrophil elastase and eventual emphysema; second only to cystic fibrosis as most common lethal genetic disorder among Caucasians of northern European ancestry. ( CSP )]
UMLS (CSP) C0221757- Disease or Syndrome
Relation/PAR: Connective Tissue Disease
Congenital Metabolic Disorder
Congenital Metabolic Disorder
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