View disease #00002

Official abbreviation Variation
Name Variation
OMIM ID -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 85 genes ACTA2, AHR, APEX1, ARID5B, ATXN2, AUTS2, BACH2, BCL2L12, BLOC1S5-TXNDC5, BMP6, C1QTNF6, C9orf3, CASP7, CDH1, CDK5RAP1, CLEC11A, COMT, CPVL, CTLA4, CYP2C9, 65 more...ACTA2, AHR, APEX1, ARID5B, ATXN2, AUTS2, BACH2, BCL2L12, BLOC1S5-TXNDC5, BMP6, C1QTNF6, C9orf3, CASP7, CDH1, CDK5RAP1, CLEC11A, COMT, CPVL, CTLA4, CYP2C9, DEF8, DNAH5, ESR1, FANCA, FARP2, FOXO3, FOXP1, GAGE1, GAGE10, GSTP1, GZMB, HCG9, HERC2, ICA1, IFIH1, IFNE, IKZF4, IL1RAPL1, IL2RA, IRF3, KITLG, LPP, LTA, MBL2, MIR31HG, MTHFR, NEK6, NOS2, NPY, PLCB3, PPP3CA, PSMB8, PSMB9, PTPN22, PTPRC, RAB5C, RALY, RERE, RPGRIP1L, SH2B3, SLC1A2, SLC44A4, SMOC2, SOD2, SOD3, STRN3, TAP1, TAP2, TBC1D2, TEF, TG, TGFBR2, TICAM1, TLR2, TLR4, TLR7, TNFRSF10A, TNFRSF11A, TSLP, TXNDC5, UBASH3A, UBE2E2, UVRAG, ZMIZ1, ZNRD1-AS1