Disease #02801 (FHL3 (lymphohistiocytosis, hemophagocytic, familial, type 3 (FHL-3)), OMIM:608898)

Official abbreviation FHL3
Name lymphohistiocytosis, hemophagocytic, familial, type 3 (FHL-3)
OMIM ID 608898
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene UNC13D
Associated tissues -
Disease features -
Remarks -

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