Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11005
Gene Symbol: SPINK5
SPINK5
CUI: C0745091
Disease: Hypereosinophilia
Hypereosinophilia
0.110 GeneticVariation 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