Disease: Hypereosinophilia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0745091
Disease: Hypereosinophilia
Hypereosinophilia 		0.110 GeneticVariation disease BEFREE Mutation in SPINK5 causes Netherton syndrome, a rare recessive skin disease that is accompanied by severe atopic manifestations including atopic dermatitis, allergic rhinitis, asthma, high serum IgE and hypereosinophilia. 19534795 2009
CUI: C0745091
Disease: Hypereosinophilia
Hypereosinophilia 		0.110 Biomarker disease HPO