Congenital heart disease

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL HEART DISEASE
C0152021MONDO:0005453EFO_0005207
USP34 Unknown
23665959 27843126 29555671 30800044 32368696 33995476
ClinGen, Disgenet, GWAS catalog
USP43 Unknown — Disgenet
USP44 Unknown
27796757 32368696 33084842 35373735
ClinGen, Disgenet, GWAS catalog
WDR5 Unknown
18932069 30377171 33131162 33442022
ClinGen, Disgenet
YTHDC2 Unknown
33201861
GWAS catalog —
ZFPM1 Unknown
14614148 16316643 28422132 30293987 34328347
ClinGen, Disgenet, HPO
All172 Causal21 Unknown156
Related Diseases Diseases that share the most curated genes with Congenital heart disease.
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Tetralogy of fallot 45 shared genesANKRD11, TBX1, NR2F2, GATA4, NOTCH1, HAND1, MCTP2, NKX2-6, NRP1, RBFOX2, ROBO1, TBX5 +33 more Related via 45 shared genes including ANKRD11, TBX1, NR2F2. Congenital heart defects 26 shared genesTBX1, UFD1, GATA4, CDK13, FOXP1, TGFB2, VEGFA, RCAN1, POU5F1, NPPB, PITX2, AHR +14 more Related via 26 shared genes including TBX1, UFD1, GATA4. Ventricular septal defect 15 shared genesTBX1, GATA4, NKX2-6, TBX5, BMP7, NFATC1, GATA5, TBX20, NKX2-5, COL1A2, ISL1, CITED2 +3 more Related via 15 shared genes including TBX1, GATA4, NKX2-6. Conotruncal cardiac defect 15 shared genesTBX1, CDH13, FOXP2, NKX2-6, CARTPT, MAP1B, AHR, NKX2-5, IQCJ, IQCJ-SCHIP1, SCHIP1, ADAM29 +3 more Related via 15 shared genes including TBX1, CDH13, FOXP2. Craniofacial abnormalities 17 shared genesFGF8, TBX1, UFD1, NOTCH1, FOXP2, TGFB2, RCAN1, PITX2, AHR, STRA6, PTCH1, LRP2 +5 more Related via 17 shared genes including FGF8, TBX1, UFD1.