A heterogeneous group of disorders with the common feature of prolonged eosinophilia of unknown cause and associated organ system dysfunction, including the heart, central nervous system, kidneys, lungs, gastrointestinal tract, and skin. There is a massive increase in the number of EOSINOPHILS in the blood, mimicking leukemia, and extensive eosinophilic infiltration of the various organs.

Descriptor ID	D017681
MeSH Number(s)	C15.378.553.231.549
Concept/Terms	Hypereosinophilic Syndrome Hypereosinophilic Syndrome Hypereosinophilic Syndromes Syndrome, Hypereosinophilic Syndromes, Hypereosinophilic Leukemia, Eosinophilic Leukemia, Eosinophilic Eosinophilic Leukemia Eosinophilic Leukemias Leukemias, Eosinophilic Loeffler's Endocarditis Loeffler's Endocarditis Loefflers Endocarditis Endocarditis, Loeffler's Endocarditis, Loefflers Loeffler Endocarditis Endocarditis, Loeffler Idiopathic Hypereosinophilic Syndrome Idiopathic Hypereosinophilic Syndrome Hypereosinophilic Syndromes, Idiopathic Idiopathic Hypereosinophilic Syndromes Syndrome, Idiopathic Hypereosinophilic Syndromes, Idiopathic Hypereosinophilic Hypereosinophilic Syndrome, Idiopathic

Below are MeSH descriptors whose meaning is more general than "Hypereosinophilic Syndrome".

Below are MeSH descriptors whose meaning is related to "Hypereosinophilic Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Hypereosinophilic Syndrome".