The typical clinical manifestations by organ type that have been reported in cases of Farber Disease (FD) and SMA-PME in the published literature. FD symptoms organized by neurological symptoms, ophthalmic symptoms, cardinal triad symptoms, respiratory symptoms, hematopoietic symptoms, gastrointestinal involvement, dermatological manifestations, liver disease, motor neuron and muscle weakness, and bone disease phenotypes | Yu, F., Amintas, S., Levade, T., & Medin, J. A. (2018). Acid ceramidase deficiency: Farber disease and SMA-PME. Orphanet journal of rare diseases, 13(1), 121. https://doi.org/10.1186/s13023-018-0845-z

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