A sphingolipidosis subtype that is characterized by the histological appearance of granulomatous deposits in tissues. It results from the accumulation of CERAMIDES in various tissues due to an inherited deficiency of ACID CERAMIDASE.
Also Known As:
Acid Ceramidase Deficiency; Ceramidase Deficiency; Farber Disease; Farber's Disease; N-Laurylsphingosine Deacylase Deficiency; Acid Ceramidase Deficiencies; Ceramidase Deficiencies; Ceramidase Deficiency, Acid; Deficiencies, Ceramidase; Deficiencies, N-Laurylsphingosine Deacylase; Deficiency, Acid Ceramidase; Deficiency, Ceramidase; Deficiency, N-Laurylsphingosine Deacylase; Disease, Farber's; Diseases, Farber's; Farber's Diseases; Farbers Disease; Lipogranulomatosis, Farber; N Laurylsphingosine Deacylase Deficiency; N-Laurylsphingosine Deacylase Deficiencies