NR2F2 related multiple congenital anomalies/dysmorphic syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
NR2F2 related multiple congenital anomalies/dysmorphic syndrome
NR2F2 Unknown — ClinGen —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with NR2F2 related multiple congenital anomalies/dysmorphic syndrome.
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46,xx sex reversal 1 shared geneNR2F2 Related via 1 shared gene including NR2F2. Atrioventricular septal defect 1 shared geneNR2F2 Related via 1 shared gene including NR2F2. Female infertility 1 shared geneNR2F2 Related via 1 shared gene including NR2F2. Tetralogy of fallot 1 shared geneNR2F2 Related via 1 shared gene including NR2F2. Congenital heart disease 1 shared geneNR2F2 Related via 1 shared gene including NR2F2.