Feingold syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FEINGOLD SYNDROME 1
164280
MYCN Unknown — HPO
FEINGOLD SYNDROME TYPE 1
391641C4551774MONDO:0008115
MYCN Causal
15821734 16906565 18671284 18470948 20301770
ClinVar, Disgenet, GWAS catalog, Orphanet, ClinGen
TTN Causal — Disgenet
All2 Causal2 Unknown1
Related Diseases Diseases that share the most curated genes with Feingold syndrome.
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Progressive contractures limb-girdle weakness muscle dystrophy syndrome 1 shared geneTTN Related via 1 shared gene including TTN. Early-onset myopathy with fatal cardiomyopathy 1 shared geneTTN Related via 1 shared gene including TTN. myopathy, myofibrillar, 9, with early respiratory failure 1 shared geneTTN Related via 1 shared gene including TTN. tibial muscular dystrophy 1 shared geneTTN Related via 1 shared gene including TTN. dilated cardiomyopathy 1G 1 shared geneTTN Related via 1 shared gene including TTN.