Farber lipogranulomatosis https://github.com/monarch-initiative/mondo/issues/5881 https://www.malacards.org/card/farber_lipogranulomatosis Farber disease NANDO:1200086 OMIM:228000 MESH:D055577 Farber's disease Farber lipogranulomatosis A rare sphingolipid disorder characterized by a spectrum of clinical signs ranging from the classical triad of painful and progressively deformed joints, subcutaneous nodules, and progressive hoarseness (due to laryngeal involvement) that presents in infancy, to varying phenotypes with respiratory and neurologic involvement. ICD9:272.8 Orphanet:333 MONDO:0009218 UMLS:C0268255 AC deficiency N-Laurylsphingosine deacylase deficiency FRBRL acid ceramidase deficiency SCTID:79935000 N-LAURYLSPHINGOSINE deacylase deficiency DOID:0050464 NANDO:2200565 ceramidase deficiency GARD:0006426 NCIT:C84710 MEDGEN:78654 subcutaneous tissue disorder ASAH1-related sphingolipidosis