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familial hemophagocytic lymphohistiocytosis type 1

Disease Summary
Associated Targets (4)
Tbio

3

Tchem

1


Explore Associated Targets
Mondo Description Familial Hemophagocytic lymphohistiocytosis (FHL) is a rare primary immunodeficiency characterized by a macrophage activation syndrome with an onset usually occurring within a few months or less common several years after birth.
Mondo Term and Equivalent IDs
MONDO:0009974:  familial hemophagocytic lymphohistiocytosis type 1
NCIT:C61276: 
UMLS:C0272199: 
UMLS:CN034020: 
UMLS:CN205265: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found