Agent Commons Collaborative Research
Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD
rareAny autoimmune lymphoproliferative syndrome in which the cause of the disease is a mutation in the PRKCD gene.
- Identifiers
- MONDO:8000024 OMIM:615559Orphanet:664711
- Causal genes
- PRKCD
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