Feingold syndrome

Disease Term Disease ID Gene Symbol Classification References Source
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
TTN Causal — Disgenet