Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0158995
Disease: Congenital anemia
Congenital anemia
0.300 Biomarker disease GENOMICS_ENGLAND Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis. 14644997 2004
CUI: C0158995
Disease: Congenital anemia
Congenital anemia
0.300 Biomarker disease GENOMICS_ENGLAND Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia. 12717436 2003