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Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is an autosomal recessive variation in the RHOG gene.
No clinical trials have been registered for hemophagocytic lymphohistiocytosis due to RhoG deficiency.
1 publication has been identified in PubMed for hemophagocytic lymphohistiocytosis due to RhoG deficiency. Research spans Epidemiology / Natural History (100%).
Dou L (2025). [PMID: 40536720](https://pubmed.ncbi.nlm.nih.gov/40536720/). *Ann Hematol*. [Epidemiology / Natural History]
Data assembled from 2 of 12 sources · Last updated Sep 21, 2026, 4:54 AM UTC