Persistent eosinophilia with organ damage.
- Specialty
- Hematology
- Subspecialty
- Hematology / Myeloid neoplasms
- Sex & age distribution
- Male: affected; Female: affected; Children: rare
- Gene(s) involved
- FIP1L1-PDGFRA
- Alternative names & eponyms
- HES
Etiology & mechanism
FIP1L1-PDGFRA or idiopathic.
Gene(s) involved (1)
Symptoms & signs (7)
In plain terms, someone with Hypereosinophilic syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
3 shared
Churg–Strauss syndrome
eosinophilia, heart failure, neuropathy
2 shared
Eosinophilia–myalgia syndrome
eosinophilia, neuropathy
2 shared
Gulf War syndrome
fatigue, rash
2 shared
Katayama syndrome
cough, eosinophilia
2 shared
Loeffler syndrome
cough, eosinophilia
2 shared
Sjögren syndrome
fatigue, neuropathy
1 shared
Abetalipoproteinemia
neuropathy
1 shared
Acute chest syndrome
cough
1 shared
Anomalous left coronary artery from pulmonary artery
heart failure
1 shared
Atypical hemolytic uremic syndrome
fatigue
Shares genes with
None.
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