Transthyretin (TTR) related cardiac amyloidosis is a progressive infiltrative cardiomyopathy that mimics hypertensive, hypertrophic heart disease and often goes undiagnosed. In the United States, the hereditary form disproportionately afflicts Black Americans, who when compared to Caucasians with wild type TTR amyloidosis, a phenotypically similar condition, present with more advanced disease despite having a non-invasive method for early identification (genetic testing). While reasons for this are unclear, this begs to consider the inadequate access to care, societal factors or a biological basis. In an effort to improve awareness and explore unique characteristics, we review the pathophysiology, epidemiology and therapeutic strategies for TTR amyloidosis, and highlight diagnostic pitfalls and clinical pearls for identifying patients with amyloid heart disease.