disease arises from feature disease has basis in feature Autoimmunity type IV hypersensitivity disease autoimmune disease lymphoid hemopathy lymphoproliferative syndrome autoimmune lymphoproliferative syndrome https://github.com/monarch-initiative/mondo/issues/9097 NANDO:2200726 GARD:0008686 Canale-Smith syndrome ICD10CM:D89.82 FAS deficiency CSP:1560-5548 NCIT:C37864 icd11.foundation:1072688797 MedDRA:10069521 ALPS (autoimmune lymphoproliferative syndrome) ALPS MONDO:0017979 NANDO:1200352 MESH:D056735 Autoimmune lymphoproliferative syndrome (ALPS) is a rare, inherited disorder characterized by non-malignant lymphoproliferation, multilineage cytopenias, and a lifelong increased risk of Hodgkin's and non-Hodgkin's lymphoma. Orphanet:3261 autoimmune lymphoproliferative syndrome type 1, autosomal dominant DOID:6688 neoplastic syndrome