Any autoimmune lymphoproliferative syndrome in which the cause of the disease is a mutation in the PRKCD gene.
Comprehensive, easy-to-understand information about this condition
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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
Castleman-Kojima disease
MONDO:0018702