familial hemophagocytic lymphohistiocytosis 2
Disease
familial hemophagocytic lymphohistiocytosis 2
- Definition
A hemophagocytic lymphohistiocytosis that has_material_basis_in an autosomal recessive mutation of the PRF1 gene on chromosome 10q22.1.
- Synonyms
- Cross References
- Parent Terms
- Child Terms
- None
- Sources of Associations
Associated Genes
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