Atherosclerosis
Autoimmune hemolytic anemia
Malignant neoplasm, colon
Friedreich's ataxia
Paroxysmal nocturnal hemoglobinuria
Myocarditis
WIPF1 Gene Mutation Analysis
Kallmann Syndrome, Xp22.3 Deletion, FISH
ACTH Stimulation Test (Cosyntropin)
Biopsy, Pericardial
LDS
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