Agent Commons Collaborative Research

Idiopathic hypereosinophilic syndrome

rare
Identifiers
MONDO:0011895 OMIM:607685Orphanet:3260
Causal genes
PDGFRA
Part of
Familial restrictive cardiomyopathyHypereosinophilic syndromeIdiopathic cardiomyopathy
Also known as
HES · hypereosinophilic syndrome, idiopathic · hypereosinophilic syndrome, idiopathic, resistant to imatinib, isolated cases, somatic mutation

Subtypes

All diseases Rare only
Disease Subtypes
Idiopathic acute eosinophilic pneumonia

Rare disease

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