has characteristic has characteristic inborn error of immunity hereditary disease hemophagocytic syndrome hereditary hemophagocytic lymphohistiocytosis GARD:0006589 UMLS:C0272199 familial hemophagocytic lymphohistiocytosis MEDGEN:78797 MedDRA:10070904 primary hemophagocytic lymphohistiocytosis ICD9:238.79 Orphanet:540 OMIMPS:267700 An instance of hemophagocytic lymphohistiocytosis that is caused by an inherited genomic modification in an individual. MONDO:0015541 genetic hemophagocytic lymphohistiocytosis genetic hemophagocytic syndrome SCTID:398250003 inherited