NKX2.5-related congenital, conduction and myopathic heart disease

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
NKX2.5-related congenital, conduction and myopathic heart disease
NKX2-5 Unknown — ClinGen
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with NKX2.5-related congenital, conduction and myopathic heart disease.
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Interrupted aortic arch 1 shared geneNKX2-5 Related via 1 shared gene including NKX2-5. Deletion 5q35 syndrome 1 shared geneNKX2-5 Related via 1 shared gene including NKX2-5. Congenital asplenia 1 shared geneNKX2-5 Related via 1 shared gene including NKX2-5. Splenic hypoplasia 1 shared geneNKX2-5 Related via 1 shared gene including NKX2-5. Congenital hypothyroidism due to absence of thyroid gland 1 shared geneNKX2-5 Related via 1 shared gene including NKX2-5.