Hirschsprung disease, cardiac defects, and autonomic dysfunction

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Subtype of: Hirschsprung disease
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Hirschsprung disease, cardiac defects, and autonomic dysfunction
MONDO_0018309
ECE1 Causal
9915973
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Hirschsprung disease, cardiac defects, and autonomic dysfunction.
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Autonomic nervous system disease 1 shared geneECE1 Related via 1 shared gene including ECE1. Congenital heart defects 1 shared geneECE1 Related via 1 shared gene including ECE1. Hirschsprung disease 1 shared geneECE1 Related via 1 shared gene including ECE1. Craniofacial abnormalities 1 shared geneECE1 Related via 1 shared gene including ECE1. Ischemic heart disease 1 shared geneECE1 Related via 1 shared gene including ECE1.