|
DOID:0110921 - familial hemophagocytic lymphohistiocytosis 1
Disease Ontology Definition:A hemophagocytic lymphohistiocytosis that has_material_basis_in an autosomal recessive mutation of HPLH1 on chromosome 9q21.3-q22.
Synonyms: FHL1, HLH1, HPLH1,
Echinobase Genes :
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)