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Diseases

Hypereosinophilic Syndrome

hypereosinophilic syndrome

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Hypereosinophilic Syndrome
Standard Disease Name
hypereosinophilic syndrome
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D017681
OMIM ID
No data
UMLS ID
C1540912
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A syndrome characterized by persistent eosinophilia, for which no underlying cause can be found, and which is associated with signs of organ involvement and dysfunction. This term has often been applied to cases of chronic eosinophilic leukemia. (WHO, 2001)|MSH2017_2016_08_12: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.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
07
STAT5B
signal transducer and activator of transcription 5B
signal transducer and activator of transcription 5B