Loeffler Endocarditis

Alias:
Primary Eosinophilic Endomyocardial Restrictive Cardiomyopathy
Eosinophilic Endomyocardial Disease
Eosinophilic Endocarditis
Loeffler's Endocarditis
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Loeffler Endocarditis, also known as primary eosinophilic endomyocardial restrictive cardiomyopathy, is related to primary hypereosinophilic syndrome and myeloid and lymphoid neoplasms associated with pdgfra rearrangement. An important gene associated with Loeffler Endocarditis is FIP1L1 (Factor Interacting With PAPOLA And CPSF1), and among its related pathways/superpathways are Innate Immune System and Overview of interferons-mediated signaling pathway. Affiliated tissues include heart and thyroid, and related phenotypes are eosinophilia and restrictive cardiomyopathy
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Child
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9
86
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Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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