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Q35064189-DD5E9161-6F3F-4478-93A9-0C1D5DA704E6
Q35064189-DD5E9161-6F3F-4478-93A9-0C1D5DA704E6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35064189-DD5E9161-6F3F-4478-93A9-0C1D5DA704E6
Whole-exome sequencing reveals overlap between macrophage activation syndrome in systemic juvenile idiopathic arthritis and familial hemophagocytic lymphohistiocytosis
P2860
Q35064189-DD5E9161-6F3F-4478-93A9-0C1D5DA704E6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35064189-DD5E9161-6F3F-4478-93A9-0C1D5DA704E6
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wasDerivedFrom
10c1579bee5f281015dd3dfe406389cead673b01
P2860
XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease