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.
Farbers sjukdom
Lipogranulomatosis, Farber — Ceramidase Deficiency — Ceramidase Deficiencies — Deficiencies, Ceramidase — Deficiency, Ceramidase — Farber's Disease — Disease, Farber's — Diseases, Farber's — Farber's Diseases — Farbers Disease — N-Laurylsphingosine Deacylase Deficiency — Deficiencies, N-Laurylsphingosine Deacylase — Deficiency, N-Laurylsphingosine Deacylase — N Laurylsphingosine Deacylase Deficiency — N-Laurylsphingosine Deacylase Deficiencies — Acid Ceramidase Deficiency — Acid Ceramidase Deficiencies — Ceramidase Deficiency, Acid — Deficiency, Acid Ceramidase — Farber Disease