hemophagocytic lymphohistiocytosis due to RhoG deficiency
MONDO:0800147Mondo
Findings
No curated finding names hemophagocytic lymphohistiocytosis due to RhoG deficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is an autosomal recessive variation in the RHOG gene.
Definition from the Mondo Disease Ontology (MONDO:0800147), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- RHOGHGNC:672
- Moderate · ClinGen · Autosomal recessive · 2024