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Echinobase
Summary Literature (0)
DOID:0110922 - familial hemophagocytic lymphohistiocytosis 2

Disease Ontology Definition:A hemophagocytic lymphohistiocytosis that has_material_basis_in an autosomal recessive mutation of PRF1 on chromosome 10q22.1.

Synonyms: FHL2, HLH2, HPLH2,

Echinobase Genes :


OMIM:
MIM:603553 - hemophagocytic lymphohistiocytosis, familial, 2; fhl2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hemophagocytic lymphohistiocytosis (is_a)