Disease #02694 (HES (hypereosinophilic syndrome, idiopathic (HES)), OMIM:607685)

Official abbreviation HES
Name hypereosinophilic syndrome, idiopathic (HES)
OMIM ID 607685
Human Phenotype Ontology Project (HPO) HPO
Inheritance Isolated Cases (Sporadic), Somatic mutation
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PDGFRA
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00047238 - PubMed: Ernst 2010 - ? - - - - - - - HES - EZH2 EZH2 1 1 Global Variome, with Curator vacancy
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