Disease #02459 (FHL-2 (lymphohistiocytosis, hemophagocytic, familial, type 2 (FHL-2)), OMIM:603553)

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Official abbreviation	FHL-2
Name	lymphohistiocytosis, hemophagocytic, familial, type 2 (FHL-2)
OMIM ID	603553
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PRF1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A