A clinicopathologic variant of multicentric Castleman's disease characterized by thrombocytopenia, ascites (anasarca), microcytic anemia, myelofibrosis, renal dysfunction, and organomegaly
Comprehensive, easy-to-understand information about this condition
Checking for content...
autoimmune lymphoproliferative syndrome type 1
MONDO:0011158
autoimmune lymphoproliferative syndrome type 2A
MONDO:0011383
autoimmune lymphoproliferative syndrome type 2B
MONDO:0011804
autoimmune lymphoproliferative syndrome type 4
MONDO:0013767
autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
MONDO:0014493
type 3 autoimmune lymphoproliferative syndrome
MONDO:8000023