Disease Term Disease ID Gene Symbol Classification References Source
PRIMARY HYPEREOSINOPHILIC SYNDROME 314950, C5679898 ETV6 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 22460074, 24577808 -
FGFR1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 22460074, 24577808 -
FIP1L1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 22460074, 24577808 -
PDGFRA Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 22460074, 24577808 -
PDGFRB Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 22460074, 24577808 -
HYPEREOSINOPHILIC SYNDROME MESH:D017681 FIP1L1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 16778211, 28347583, 31036733 -
PDGFRA Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 16778211, 28347583, 31036733 -
TNFSF8 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 8896393 -
HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC 607685 PDGFRA Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
IDIOPATHIC HYPEREOSINOPHILIC SYNDROME C0206141, MONDO:0011895 PDGFRA Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -